Hepatitis B antiviral agents

ABSTRACT

The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof:
 
X-A-Y—Z-L-R 1   (I)
 
which inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV life cycle of the hepatitis B virus and are also useful as antiviral agents. The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from HBV infection. The invention also relates to methods of treating an HBV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.

RELATED APPLICATION

This application claims priority to U.S. Application No. 62/160,946, filed May 13, 2015. The entire teachings of the above application are incorporated herein by reference.

TECHNICAL FIELD

The present invention relates generally to novel antiviral agents. Specifically, the present invention relates to compounds which can inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the function of the HBV life cycle, compositions comprising such compounds, methods for inhibiting HBV viral replication, methods for treating or preventing HBV infection, and processes for making the compounds.

BACKGROUND OF THE INVENTION

HBV infection remains a major public health problem, affecting approximately 2 billion people worldwide. Among them, 350 million people worldwide and 1.4 million in the US develop a chronic infection, which can lead to chronic persistent hepatitis, liver cirrhosis, and hepatocellular carcinoma (HCC). Every year 500,000 to 1 million people die from the end stage of liver diseases caused by HBV infection.

Despite the availability of a prophylactic HBV vaccine, the burden of chronic HBV infection continues to be a significant unmet worldwide medical problem, due to suboptimal treatment options and sustained rates of new infections in most parts of the developing world. Current treatments do not provide a cure and are limited to only two classes of agents (interferon and nucleoside analogues/inhibitors of the viral polymerase); drug resistance, low efficacy, and tolerability issues limit their impact. The low cure rates of HBV are attributed at least in part to the presence and persistence of covalently closed circular DNA (cccDNA) in the nucleus of infected hepatocytes. However, persistent suppression of HBV DNA slows liver disease progression and helps to prevent HCC. Current therapy goals for HBV-infected patients are directed to reducing serum HBV DNA to low or undetectable levels, and to ultimately reducing or preventing the development of cirrhosis and HCC.

The HBV is an enveloped, partially double-stranded DNA (dsDNA) virus of the hepadnavirus family (Hepadnaviridae). HBV capsid protein (CP) plays essential roles in HBV replication. The predominant biological function of capsid protein is to act as a structural protein to encapsidate pre-genomic RNA and form immature capsid particles, which spontaneously self-assemble from many copies of core dimers in the cytoplasm. Capsid protein also regulates viral DNA synthesis through different phosphorylation status of its C-terminal phosphorylation sites. Also, capsid protein might facilitate the nuclear translocation of viral relaxed circular genome by means of the nuclear localization signals located in the Arginine-rich domain of the C-terminal region of capsid protein. In the nucleus, as a component of viral cccDNA minichromosome, capsid protein could play a structural and regulatory role in the functionality of cccDNA minichromosomes. Capsid protein also interacts with viral large envelope protein in endoplasmic reticulum (ER) and triggers the release of intact viral particles from hepatocytes.

Capsid related anti-HBV inhibitors have been reported. For example, phenylpropen-amide derivatives, including compounds named AT-61 and AT-130 (Feld J. et al., Antiviral Res. 2007, 76, 168), and a class of thiazolidin-4-ones from Valeant (WO2006/033995), have been shown to inhibit pregenomic RNA (pgRNA) packaging. Heteroaryldihydropyrimidines or HAPs were discovered in a tissue culture-based screening (Weber et al., Antiviral Res. 2002, 54, 69). These HAP analogs act as synthetic allosteric activators and are able to induce aberrant capsid formation that leads to degradation of the core protein. A subclass of sulphamoyl-arylamides also shows activity against HBV (WO2013/006394, WO2013/096744, and WO 2014184365). It was also shown that the small molecule bis-ANS acts as a molecular ‘wedge’ and interferes with normal capsid-protein geometry and capsid formation (Zlotnick A. et al. J. Virol. 2002, 4848).

There is a need in the art for novel therapeutic agents that treat, ameliorate or prevent HBV infection. Administration of these therapeutic agents to an HBV infected patient, either as monotherapy or in combination with other HBV treatments or ancillary treatments, will lead to significantly improved prognosis, diminished progression of the disease, and enhanced seroconversion rates.

SUMMARY OF THE INVENTION

The present invention relates to novel antiviral compounds, pharmaceutical compositions comprising such compounds, as well as methods to treat or prevent viral (particularly HBV) infection in a subject in need of such therapy with said compounds. Compounds of the present invention inhibit the protein(s) encoded by hepatitis B virus (HBV) or interfere with the life cycle of HBV and are also useful as antiviral agents. In addition, the present invention includes the process for the preparation of the said compounds.

In its principal aspect, the present invention provides a compound of Formula (I): X-A-Y—Z-L-R₁  (I) or a pharmaceutically acceptable salt thereof, wherein:

X is an optionally substituted aryl or optionally substituted heteroaryl; preferably X is an optionally substituted phenyl; in one embodiment, X is a halogen-substituted phenyl, preferably a fluoro-substituted phenyl, such as 3,4,5-trifluorophenyl;

A is absent, —NHCO— or optionally substituted azolyl;

Y is an optionally substituted arylamino (-aryl-NH—) or optionally substituted heteroarylamino (-heteroaryl-NH—); wherein the said amino group is directly connected to A (or X when A is absent) or Z; in one embodiment Y is optionally substituted phenylamino; in another embodiment, Y is an optionally substituted azolylamino group; in yet another embodiment, Y is an optionally substituted bicyclic arylamino group; in yet another embodiment, Y is an optionally substituted bicyclic azolylamino group;

Alternatively, X and A are taken together to form an optionally substituted fused bicyclic azolyl group; wherein the five-membered azolyl ring is connected to Y; preferably X and A are taken together to form an optionally substituted benzimidazolyl group or optionally substituted indazolyl group;

Alternatively, Y and A are taken together to form an optionally substituted fused bicyclic azolylamino group; wherein the said amino group is connected to X; preferably Y and A are taken together to form an optionally substituted benzimidazolylamino group or indazolylamino group;

Z is —S(O)₂—, —C(O)—, or —C(O)C(O)—;

L is —NR₂—, O or —CR₁R₂—; and

R₁ and R₂ at each occurrence are each independently selected from the group of consisting of hydrogen, optionally substituted —C₁-C₈ alkyl, optionally substituted —C₂-C₈ alkenyl, optionally substituted —C₂-C₈ alkynyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted 3- to 8-membered heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; alternatively, R₁ and R₂ are taken together with the atom to which they are attached to form an optionally substituted C₃-C₈ cycloalkyl or an optionally substituted 3- to 8-membered heterocyclic; in one embodiment, L is —NR₂, and R₁, R₂ and the nitrogen atom are taken together to form a substituted or unsubstituted piperidinyl group, such as a 4-hydroxypiperidin-1-yl group.

Each preferred group stated above can be taken in combination with one, any or all other preferred groups.

DETAILED DESCRIPTION OF THE INVENTION

In one embodiment of the present invention is a compound of Formula (I) as described above, or a pharmaceutically acceptable salt thereof.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein A is —NHC(O)—. In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein A is an optionally substituted azolyl.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein A is an optionally substituted imidazolyl, optionally substituted pyrazolyl, or optionally substituted triazolyl.

In another particular embodiment, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein A is an azolyl group derived from one of the following, or a tautomer thereof, by removal of two hydrogen atoms:

wherein each of the above shown azole groups is optionally substituted when possible and may be connected to groups X and Y through either carbon or nitrogen.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl. In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted monocyclic heteroaryl. In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted bicyclic heteroaryl.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted benzimidazolyl, benzothiazolyl, benzoxazolyl, indazolyl, quinolyl, isoquinolyl or quinazolyl.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salt thereof, wherein Y is optionally substituted phenylamino. In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein Y is optionally substituted monocyclic heteroarylamino. In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein Y is optionally substituted bicyclic heteroarylamino.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl and Y is optionally substituted monocyclic heteroarylamino.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X is optionally substituted monocyclic heteroaryl and Y is optionally substituted phenylamino.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein X and Y are each independently and optionally substituted with one to three substituents selected from the group consisting of halo, CN, and optionally substituted methyl.

In one embodiment Y is connected to A in Formula (I) via the exocyclic amino group and Y is connected to Z through a carbon atom which belongs to an aryl or heteroaryl ring. In yet another embodiment Y is connected to Z in Formula (I) via the exocyclic amino group and Y is connected to A through a carbon atom which belongs to an aryl or heteroaryl group.

In the embodiments above, Y is preferably selected from the groups set forth below, which can be optionally substituted, by removal of one hydrogen atom, wherein the second connection point of Y can be at any carbon atom of the phenyl or heteroaryl ring:

In the embodiments above, Y is preferably selected from the groups set forth below, which can be optionally substituted, by removal of one hydrogen atom, wherein the second connection point of Y can be at any carbon atom of the phenyl or heteroaryl ring:

In certain embodiments, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is —S(O)₂—. In certain embodiments, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein Z is —C(O)—. In certain embodiments, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, Z is —C(O)C(O)—.

In another embodiment, the compound of Formula (I) is represented by Formula (IIa), (In), or (IIc), or a pharmaceutically acceptable salt thereof:

wherein one U is N or NR₁₁, another U is N, NR₁₁, or CR₁₂, and the third U is O, S, N, NR₁₁, or CR₁₂; R₁₁ at each occurrence is each independently selected from the groups consisting of hydrogen, optionally substituted —C₁-C₆ alkyl and optionally substituted —C₃-C₈ cycloalkyl; R₁₂ at each occurrence is independently selected from the groups consisting of hydrogen, halo, —CN, —NO₂, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₁-C₆ alkoxy and optionally substituted —C₃-C₈ cycloalkyl; X, R₁ and R₂ are as previously defined. It is to be understood that the definitions of U in any given embodiment are selected such that the ring comprising the three U units is aromatic.

In another embodiment, the compound of Formula (I) is represented by Formulae (IIa-1)-(IIa-8), (IIb-1)-(IIb-8), or (IIc-1)-(IIc-8), or a pharmaceutically acceptable salt thereof:

wherein V is O, NR₁₁, or S; V′ is N or CR₁₂, and X, R₁, R₂, R₁₁ and R₁₂ are as previously defined. It is to be understood that the definitions of V and V′ in any given embodiment are selected such that the ring containing the group V and V′ is aromatic.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formulae (IIa-1)-(IIa-8), (IIb-1)-(IIb-8), or (IIc-1)-(IIc-8), or a pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl, optionally substituted monocyclic heteroaryl or optionally substituted bicyclic heteroaryl.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formulae (IIa-1)-(IIa-8), (IIb-1)-(IIb-8), or (IIc-1)-(IIc-8), or a pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl, optionally substituted naphthyl, optionally substituted pyridyl, optionally substituted pyrimidinyl, optionally substituted thiophenyl, optionally substituted thiazolyl, optionally substituted thiadiazolyl, optionally substituted oxazolyl, optionally substituted isoxazolyl, optionally substituted oxadiazolyl, optionally substituted imidiazolyl, optionally substituted pyrazolyl, optionally substituted triazolyl, or optionally substituted quinolinyl.

In another embodiment, the compound of Formula (I) is represented by Formula (IIa-5-A), (IIb-5-B), or (IIc-5-C), or a pharmaceutically acceptable salt thereof:

wherein R₁₅ is independently selected from the group consisting of hydroxy, halogen, cyano, —CO₂CH₃, —CO₂H, optionally substituted aryl, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, preferably R₁₅ is F, Cl, trifluoromethyl or cyclopropyl; R₁₆ is independently selected from optionally substituted —C₁-C₆ alkyl and optionally substituted —C₃-C₈ cycloalkyl, preferably R₁₆ is methyl; m at each occurrence is each independently 0, 1, 2, 3, 4 or 5; and R₁, R₂, are as previously defined.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formula (IIa-5-A), (IIb-5-B), or (IIc-5-C), or a pharmaceutically acceptable salts thereof, wherein R₁₅ at each occurrence is each independently selected from halogen, preferably fluorine; and m is 2 or 3.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formula (IIa-5-A), (IIb-5-B), or (IIc-5-C), or a pharmaceutically acceptable salts thereof, wherein R₁ and R₂ are taken together with the nitrogen atom to which they are attached to form an optionally substituted 3- to 8-membered heterocyclic, preferably the said 3- to 8-membered heterocyclic is an optionally substituted piperidinyl group, more preferably, it is a 4-hydroxypiperidin-1-yl group.

In another embodiment, the compound of Formula (I) is represented by Formula (IIIa), (IIIb), or (IIIc), or a pharmaceutically acceptable salt thereof:

wherein each U, X, R₁ and R₂ are as previously defined. It is to be understood that the definitions of U in any given embodiment are selected such that the ring comprising the three U units is aromatic.

In another embodiment, the compound of Formula (I) is represented by Formulae (IIIa-1)-(IIIa-8), (IIIb-1)-(IIIb-8), or (IIIc-1)-(IIIc-8), or a pharmaceutically acceptable salt thereof:

wherein V, V′, X, R₁, R₂, R₁₁ and R₁₂ are as previously defined. It is to be understood that the definitions of V and V′ in any given embodiment are selected such that the ring containing the group V and V′ is aromatic.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formulae (IIIa-1)-(IIIa-8), (IIIb-1)-(IIIb-8), or (IIIc-1)-(IIIc-8), or a pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl, optionally substituted monocyclic heteroaryl or optionally substituted bicyclic heteroaryl.

In certain embodiments, the present invention relates to compounds of Formula (I) represented by Formulae (IIIa-1)-(IIIa-8), (IIIb-1)-(IIIb-8), or (IIIc-1)-(IIIc-8), or a pharmaceutically acceptable salts thereof, wherein X is optionally substituted phenyl, optionally substituted naphthyl, optionally substituted pyridyl, optionally substituted pyrimidinyl, optionally substituted thiophenyl, optionally substituted thiazolyl, optionally substituted thiadiazolyl, optionally substituted oxazolyl, optionally substituted isoxazolyl, optionally substituted oxadiazolyl, optionally substituted imidiazolyl, optionally substituted pyrazolyl, optionally substituted triazolyl, or optionally substituted quinolinyl.

In another embodiment, the compound of Formula (I) is represented by Formula (IVa), (IVb), or (IVc), or a pharmaceutically acceptable salt thereof:

wherein W at each occurrence is independently selected from N or CR₁₄; preferably 0 to 3 W's are N; R₁₄ at each occurrence is each independently selected from the groups consisting of hydrogen, hydroxy, protected hydroxy, halo, —CN, —NO₂, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₂-C₈ alkenyl, optionally substituted —C₂-C₈ alkynyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted 3- to 8-membered heterocyclic, optionally substituted —C₁-C₆ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl; X, R₁, and R₂ are as previously defined.

In another embodiment, the compound of Formula (I) is represented by Formula (IVa-1), (IVb-1), or (IVc-1), or a pharmaceutically acceptable salt thereof:

wherein m at each occurrence is each independently 0, 1, 2, 3 or 4; X, R₁, R₂ and R₁₄ are as previously defined.

In another embodiment, the compound of Formula (I) is represented by Formula (Va), (Vb), or (Vc), or a pharmaceutically acceptable salt thereof:

wherein each W is independently selected from N or CR₁₄; preferably 0 to 3 W's are N; X, R₁, R₂, R₁₄ are as previously defined.

In another embodiment, the compound of Formula (I) is represented by Formula (Va-1), (Vb-1), or (Vc-1), or a pharmaceutically acceptable salt thereof:

wherein X, R₁, R₂, R₁₄ are as previously defined.

In another embodiment, the compound of Formula (I) is represented by Formula (VIa), (VIb), (VIc), (VIa′), (VIb′), or (VIc′), or a pharmaceutically acceptable salt thereof:

wherein one Q is N or NR₁₁, the other Q is O, S, N, NR₁₁ or CR₁₂, and W is as previously defined, provided that W is C when attached to the carbonyl group (VIb, VIc, VIb′, VIc′) or the sulfonyl group (VIa, VIa′); X, R₁, R₂, R₁₁, R₁₂, and R₁₄ are as previously defined; provided R₁₄ can be replaced with the bond to the sulfonyl group or the carbonyl group respectively.

In another embodiment, the compound of Formula (I) is represented by Formula (VIa-1), (VIb-1), (VIc-1), (VIa′-1), (VIb′-1), or (VIc′-1), or a pharmaceutically acceptable salt thereof:

wherein Q is NR₁₁, O, S or CR₁₂; m, R₁, R₂, R₁₁, R₁₂ and R₁₄ are as previously defined. The invention further includes compounds of Formulas (VIa-1), (VIb-1), (VIc-1), (VIa′-1), (VIb′-1), and (VIc′-1) in which the positions of Q and the nitrogen atom in the five-membered ring are interchanged, provided that the resulting five-membered ring is aromatic.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein A-Y are taken together to represent a system selected from the following:

wherein each of the above shown core groups is optionally substituted and each CH in each phenyl or heteroaryl ring can be independently replaced with an N if possible.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein A-Y are taken together to represent a system selected from the following:

wherein each of the above shown core group is optionally substituted and each CH in each phenyl or heteroaryl ring can be independently replaced with an N if possible.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein A-Y are taken together to represent a polycyclic system selected from the following:

wherein each of the above shown core groups is optionally substituted and up to 3 CH's in each phenyl or heteroaryl ring can be independently replaced with an N if possible.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein X-A-Y are taken together to form a polycyclic system selected from the following:

wherein each of the above shown core groups is optionally substituted and up to three CH's in each phenyl or heteroaryl ring can be independently replaced with an N if possible.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein X-A-Y are taken together to form a polycyclic system selected from the following:

wherein each of the above shown core groups is optionally substituted and up to three CH's in each phenyl or heteroaryl ring can be replaced with an N if possible.

In still another embodiment, the invention relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein X-A-Y are taken together to form a polycyclic system selected from the following:

wherein each of the above shown core group is optionally substituted and up to three CH's in each phenyl or heteroaryl ring can be replaced with a N if possible.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is —NR₂, wherein R₂ is as previously defined.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is O.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is —NR₂, wherein R₂ is —C₁-C₈ alkyl, —C₃-C₈ cycloalkyl, or 3- to 8-membered heterocyclic, each optionally substituted with one, two or three groups independently selected from hydroxy, protected hydroxy, halo, —CN, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl.

In certain embodiments, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein R₁ is —C₁-C₈ alkyl, —C₃-C₈ cycloalkyl, or 3- to 8-membered heterocyclic, each optionally substituted with one, two or three groups independently selected from hydroxy, protected hydroxy, halo, —CN, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl.

In another embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is —NH or —CH₂.

In another embodiment, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein L is —NH; R₁ is optionally substituted arylalkyl or optionally substituted heteroarylalkyl.

In another embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is —NH; R₁ is arylalkyl or heteroarylalkyl, each optionally substituted with one, two or three groups independently selected from hydroxy, protected hydroxy, halo, —CN, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl.

In another embodiment, the present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof, wherein L is —NR₂ and R₂ is optionally substituted arylalkyl or optionally substituted heteroarylalkyl.

In another embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein L is —NR₂, and R₂ is arylalkyl or heteroarylalkyl, each optionally substituted with one, two or three groups independently selected from hydroxy, protected hydroxy, halo, —CN, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl.

In another particular embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein -L-R₁ taken together represents a C₃-C₈ cycloalkyl or optionally substituted 3- to 8-membered heterocyclic.

In another particular embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein -L-R₁ taken together represents a C₃-C₈ cycloalkyl or 3- to 8-membered heterocyclic containing one or two heteroatoms selected from N, O and S; each optionally substituted with one, two or three groups independently selected from hydroxy, protected hydroxy, halo, —CN, amino, protected amino, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy, —C(O)₂—C₁-C₆ alkyl, —C(O)NH—C₁-C₆ alkyl, and —C(O)—C₁-C₆ alkyl.

In another particular embodiment, the present invention relates to compounds of Formula (I), and pharmaceutically acceptable salts thereof, wherein -L-R₁ is selected from the following:

wherein each of these groups is optionally substituted.

It will be appreciated that the description of the present invention herein should be construed in congruity with the laws and principles of chemical bonding. In some instances it may be necessary to remove a hydrogen atom in order to accommodate a substituent at any given location.

It is intended that the definition of any substituent or variable (e.g., R₁, R₂, etc.) at a particular location in a molecule be independent of its definitions elsewhere in that molecule. For example, when L-R₁ is C(R₁)₂R₂, each of the two R₁ groups may be the same or different.

It will be yet appreciated that the compounds of the present invention may contain one or more asymmetric carbon atoms and may exist in racemic, diastereoisomeric, and optically active forms. It will still be appreciated that certain compounds of the present invention may exist in different tautomeric forms. All tautomers are contemplated to be within the scope of the present invention.

In one aspect, the compounds of the invention are useful in HBV treatment by disrupting, accelerating, reducing, delaying and/or inhibiting normal viral capsid assembly and/or disassembly of immature or mature particles, thereby inducing aberrant capsid morphology and leading to antiviral effects such as disruption of virion assembly and/or disassembly, virion maturation, and/or virus egress. In one embodiment, a disruptor of capsid assembly interacts with mature or immature viral capsid to perturb the stability of the capsid, thus affecting assembly and/or disassembly. In another embodiment, a disruptor of capsid assembly perturbs protein folding and/or salt bridges required for stability, function and/or normal morphology of the viral capsid, thereby disrupting and/or accelerating capsid assembly and/or disassembly. In yet another embodiment, the compounds of the invention bind capsid and alter metabolism of cellular polyproteins and precursors, leading to abnormal accumulation of protein monomers and/or oligomers and/or abnormal particles, which causes cellular toxicity and death of infected cells. In another embodiment, the compounds of the invention cause failure of the formation of capsid of optimal stability, affecting efficient uncoating and/or disassembly of viruses (e.g., during infectivity).

In one embodiment, the compounds of the invention disrupt and/or accelerate capsid assembly and/or disassembly when the capsid protein is immature. In another embodiment, the compounds of the invention disrupt and/or accelerate capsid assembly and/or disassembly when the capsid protein is mature. In yet another embodiment, the compounds of the invention disrupt and/or accelerate capsid assembly and/or disassembly during vial infectivity. In yet another embodiment, the disruption and/or acceleration of capsid assembly and/or disassembly attenuates HBV viral infectivity and/or reduces viral load. In yet another embodiment, disruption, acceleration, inhibition, delay and/or reduction of capsid assembly and/or disassembly eradicates the virus from the host organism. In yet another embodiment, eradication of the HBV from a host advantageously obviates the need for chronic long-term therapy and/or reduces the duration of long-term therapy.

In one embodiment, the compounds described herein are suitable for monotherapy and are effective against natural or native HBV strains and against HBV strains resistant to currently known drugs. In another embodiment, the compounds described herein are suitable for use in combination therapy.

In another embodiment, the compounds of the invention can be used in methods of modulating (e.g., inhibit, disrupt or accelerate) the activity of HBV cccDNA. In yet another embodiment, the compounds of the invention can be used in methods of diminishing or preventing the formation of HBV cccDNA. In another embodiment, the compounds of the invention can be used in methods of diminishing or preventing the transcription of HBV cccDNA. In another embodiment, the additional therapeutic agent can be selected from immune modulator or immune stimulator therapies, which includes biological agents belonging to the interferon class, such as interferon alpha 2a or 2b or modified interferons such as pegylated interferon, alpha 2a, alpha 2b, lamda; or TLR modulators such as TLR-7 agonists or TLR-9 agonists; or therapeutic vaccines to stimulate an HBV-specific immune response such as virus-like particles composed of HBcAg and HBsAg, immune complexes of HBsAg and HBsAb, or recombinant proteins comprising HBx, HBsAg and HBcAg in the context of a yeast vector; or immunity activator such as SB-9200 of certain cellular viral RNA sensors such as RIG-I, NOD2, and MDA5 protein, or antiviral agents that block viral entry or maturation or target the HBV polymerase such as nucleoside or nucleotide or non-nucleos(t)ide polymerase inhibitors, or antiviral agents that modulates or inhibits the transcription of HBV cccDNA, and agents of distinct or unknown mechanism including agents that disrupt the function of other essential viral protein(s) or host proteins required for HBV replication or persistence. In an embodiment of the combination therapy, the reverse transcriptase inhibitor is at least one of Zidovudine, Didanosine, Zalcitabine, ddA, Stavudine, Lamivudine, Abacavir, Emtricitabine, Entecavir, Apricitabine, Atevirapine, ribavirin, acyclovir, famciclovir, valacyclovir, ganciclovir, valganciclovir, Tenofovir, Adefovir, PMPA, cidofovir, Efavirenz, Nevirapine, Delavirdine, or Etravirine.

In another embodiment of the combination therapy, the TLR-7 agonist is selected from the group consisting of SM360320 (9-benzyl-8-hydroxy-2-(2-methoxy-ethoxy)adenine), AZD 8848 (methyl[3-({[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl][3-(4-morpholinyl) propyl]amino Imethyl)phenyl]acetate), GS-9620 (4-Amino-2-butoxy-8-[3-(1-pyrrolidinylmethyl)benzyl]-7,8-dihydro-6(5H)-pteridinone), and RO6864018.

In an embodiment of these combination therapies, the compound and the additional therapeutic agent are co-formulated. In another embodiment, the compound and the additional therapeutic agent are co-administered.

In another embodiment of the combination therapy, administering the compound of the invention allows for administering of the additional therapeutic agent at a lower dose or frequency as compared to the administering of the at least one additional therapeutic agent alone that is required to achieve similar results in prophylactically treating an HBV infection in a subject in need thereof.

In another embodiment of the combination therapy, before administering the therapeutically effective amount of the compound of the invention, the subject is known to be refractory to a compound selected from the group consisting of a HBV polymerase inhibitor, interferon, viral entry inhibitor, viral maturation inhibitor, distinct capsid assembly modulator, antiviral compounds of distinct or unknown mechanism, and combination thereof.

In still another embodiment of the method, administering the compound of the invention reduces viral load in the subject to a greater extent compared to the administering of a compound selected from the group consisting of a HBV polymerase inhibitor, interferon, viral entry inhibitor, viral maturation inhibitor, distinct capsid assembly modulator, antiviral compounds of distinct or unknown mechanism, and combination thereof.

In another embodiment, administering of the compound of the invention causes a lower incidence of viral mutation and/or viral resistance than the administering of a compound selected from the group consisting of a HBV polymerase inhibitor, interferon, viral entry inhibitor, viral maturation inhibitor, distinct capsid assembly modulator, antiviral compounds of distinct or unknown mechanism, and combination thereof.

Definitions

Listed below are definitions of various terms used to describe this invention. These definitions apply to the terms as they are used throughout this specification and claims, unless otherwise limited in specific instances, either individually or as part of a larger group.

The term “aryl,” as used herein, refers to a mono- or polycyclic carbocyclic ring system comprising at least one aromatic ring, including, but not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, and indenyl. A polycyclic aryl is a polycyclic ring system that comprises at least one aromatic ring. Polycyclic aryls can comprise fused rings, covalently attached rings or a combination thereof.

The term “heteroaryl,” as used herein, refers to a mono- or polycyclic aromatic radical having one or more ring atom selected from S, O and N; and the remaining ring atoms are carbon, wherein any N or S contained within the ring may be optionally oxidized. Heteroaryl includes, but is not limited to, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzoxazolyl, quinoxalinyl. A polycyclic heteroaryl can comprise fused rings, covalently attached rings or a combination thereof.

In accordance with the invention, aromatic groups can be substituted or unsubstituted.

The term “bicyclic aryl” or “bicyclic heteroaryl” refers to a ring system consisting of two rings wherein at least one ring is aromatic; and the two rings can be fused or covalently attached.

The term “azole group,” as used herein, refers to 5-membered heteroaromatic ring containing at least one nitrogen atom. Preferred azole groups contain a nitrogen atom and at least one additional heteroatom, preferably a nitrogen, oxygen or sulfur atom. Azole groups include, but are not limited to pyrazole, imidazole, thiazole, oxazole, isoxazole, 1,2,3-triazole, 1,2,4-triazole, tetrazole. An azole group is termed “ortho” substituted in reference to two substituents which are on adjacent ring atoms. An azole group is termed “meta” substituted in reference to two substituents which are not on adjacent ring positions. An “azolyl” group is a univalent or bivalent group derived from an azole group by removal of one or two hydrogen atoms. Azolyl groups include, but are not limited to, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isoxazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, tetrazolyl.

The term “bicyclic azole” or “bicyclic azole group” refers to an aromatic ring system consisting of two rings wherein at least one ring is azole group; and the two rings can be fused or covalently attached. Preferred bicyclic azole groups are those in which an azole ring is fused to a six-membered aromatic or heteroaromatic ring. Such groups include, but are not limited to, benzimidazole, benzopyrazole, benzotriazole, benzoxazole, benzisoxazole benzothiazole, imidazolopyridine, pyrazolopyridine, thiazolopyridine, oxazolopyridine, isoxazolopyridine, triazolopyridine, and tetrazolopyridine. A bicyclic azolyl group is a univalent or bivalent group derived from a biclyclic azole group by removal of one or two hydrogen atoms. Such groups include, but are not limited to, benzimidazolyl, benzopyrazolyl, benzotriazolyl, benzoxazolyl, benzisoxazolyl, benzothiazolyl, imidazolopyridyl, pyrazolopyridyl, thiazolopyridyl, oxazolopyridyl, isoxazolopyridyl, triazolopyridyl, and tetrazolopyridyl. A univalent bicyclic azolyl group can be derived from the corresponding bicyclic azole group by removal of a hydrogen atom from either ring. A bivalent bicyclic azolyl group can be derived from the corresponding bicyclic azole group by removal of two hydrogen atoms from the same ring or one hydrogen atom from each ring.

The term “alkyl” as used herein, refers to saturated, straight- or branched-chain hydrocarbon radicals. “C₁-C₄ alkyl,” “C₁-C₆ alkyl,” “C₁-C₈ alkyl,” “C₂-C₄ alkyl,” or “C₃-C₆ alkyl,” refer to alkyl groups containing from one to four, one to six, one to eight carbon atoms, 2 to 4 and 3 to 6 carbon atoms respectively. Examples of C₁-C₈ alkyl radicals include, but are not limited to, methyl, ethyl, propyl, isopropyl, n-butyl, tert-butyl, neopentyl, n-hexyl, heptyl and octyl radicals.

The term “alkenyl” as used herein, refers to straight- or branched-chain hydrocarbon radicals having at least one carbon-carbon double bond by the removal of a single hydrogen atom. “C₂-C₈ alkenyl,” “C₂-C₄ alkenyl,” “C₃-C₄ alkenyl,” or “C₃-C₆ alkenyl,” refer to alkenyl groups containing from two to eight, two to four, three to four or three to six carbon atoms respectively. Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, heptenyl, octenyl, and the like.

The term “alkynyl” as used herein, refers to straight- or branched-chain hydrocarbon radicals having at least one carbon-carbon double bond by the removal of a single hydrogen atom. “C₂-C₈ alkynyl,” “C₂-C₄ alkynyl,” “C₃-C₄ alkynyl,” or “C₃-C₆ alkynyl,” refer to alkynyl groups containing from two to eight, two to four, three to four or three to six carbon atoms respectively. Representative alkynyl groups include, but are not limited to, for example, ethynyl, 1-propynyl, 1-butynyl, heptynyl, octynyl, and the like.

The term “cycloalkyl”, as used herein, refers to a monocyclic or polycyclic saturated carbocyclic ring compound, and the carbon atoms may be optionally oxo-substituted. Preferred cycloalkyl groups include C₃-C₈ cycloalkyl and C₄-C₇ cycloalkyl. Examples of C₃-C₈ cycloalkyl include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentyl and cyclooctyl; and examples of C₄-C₇ cycloalkyl include, but are not limited to, cyclopentyl, cyclohexyl, bicyclo[2.2.1]heptyl, and the like.

The term “cycloalkenyl”, as used herein, refers to monocyclic or polycyclic carbocyclic ring compound having at least one carbon-carbon double bond and the carbon atoms may be optionally oxo-substituted. Preferred cycloalkenyl groups include C₃-C₈ cycloalkenyl or C₅-C₇ cycloalkenyl groups. Examples of C₃-C₈ cycloalkenyl include, but not limited to, cyclopropenyl, cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl, and the like; and examples of C₅-C₇ cycloalkenyl include, but not limited to, cyclopentenyl, cyclohexenyl, cycloheptenyl, and the like.

As used herein, the term “arylalkyl” means a functional group wherein an alkylene chain is attached to an aryl group, e.g., —CH₂CH₂-phenyl. The term “substituted arylalkyl” means an arylalkyl functional group in which the aryl group is substituted. Similarly, the term “heteroarylalkyl” means a functional group wherein an alkylene chain is attached to a heteroaryl group. The term “substituted heteroarylalkyl” means a heteroarylalkyl functional group in which the heteroaryl group is substituted.

As used herein, the term “alkoxy” employed alone or in combination with other terms means, unless otherwise stated, an alkyl group having the designated number of carbon atoms connected to the rest of the molecule via an oxygen atom, such as, for example, methoxy, ethoxy, 1-propoxy, 2-propoxy (isopropoxy) and the higher homologs and isomers. Preferred alkoxy are (C₁-C₃) alkoxy.

It is understood that any alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclic and cycloalkenyl moiety described herein can also be an aliphatic group or an alicyclic group.

An “aliphatic” group is a non-aromatic moiety comprised of any combination of carbon atoms, hydrogen atoms, halogen atoms, oxygen, nitrogen or other atoms, and optionally contains one or more units of unsaturation, e.g., double and/or triple bonds. Examples of aliphatic groups are functional groups, such as alkyl, alkenyl, alkynyl, O, OH, NH, NH₂, C(O), S(O)₂, C(O)O, C(O)NH, OC(O)O, OC(O)NH, OC(O)NH₂, S(O)₂NH, S(O)₂NH₂, NHC(O)NH₂, NHC(O)C(O)NH, NHS(O)₂NH, NHS(O)₂NH₂, C(O)NHS(O)₂, C(O)NHS(O)₂NH or C(O)NHS(O)₂NH₂, and the like, groups comprising one or more functional groups, non-aromatic hydrocarbons (optionally substituted), and groups wherein one or more carbons of a non-aromatic hydrocarbon (optionally substituted) is replaced by a functional group. Carbon atoms of an aliphatic group can be optionally oxo-substituted. An aliphatic group may be straight chained, branched, cyclic, or a combination thereof and preferably contains between about 1 and about 24 carbon atoms, more typically between about 1 and about 12 carbon atoms. In addition to aliphatic hydrocarbon groups, as used herein, aliphatic groups expressly include, for example, alkoxyalkyls, polyalkoxyalkyls, such as polyalkylene glycols, polyamines, and polyimines, for example. Aliphatic groups may be optionally substituted.

The terms “heterocyclic” or “heterocycloalkyl” can be used interchangeably and referred to a non-aromatic ring or a bi- or tri-cyclic group fused system, where (i) each ring system contains at least one heteroatom independently selected from oxygen, sulfur and nitrogen, (ii) each ring system can be saturated or unsaturated (iii) the nitrogen and sulfur heteroatoms may optionally be oxidized, (iv) the nitrogen heteroatom may optionally be quaternized, (v) any of the above rings may be fused to an aromatic ring, and (vi) the remaining ring atoms are carbon atoms which may be optionally oxo-substituted. Representative heterocycloalkyl groups include, but are not limited to, 1,3-dioxolane, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, and tetrahydrofuryl. Such heterocyclic groups may be further substituted. Heteroaryl or heterocyclic groups can be C-attached or N-attached (where possible).

It is understood that any alkyl, alkenyl, alkynyl, alicyclic, cycloalkyl, cycloalkenyl, aryl, heteroaryl, heterocyclic, aliphatic moiety or the like, described herein can also be a divalent or multivalent group when used as a linkage to connect two or more groups or substituents, which can be at the same or different atom(s). One of skill in the art can readily determine the valence of any such group from the context in which it occurs.

The term “substituted” refers to substitution by independent replacement of one, two, or three or more of the hydrogen atoms with substituents including, but not limited to, —F, —Cl, —Br, —I, —OH, C₁-C₁₂-alkyl; C₂-C₁₂-alkenyl, C₂-C₁₂-alkynyl, protected hydroxy, —NO₂, —N₃, —CN, —NH₂, protected amino, oxo, thioxo, —NH—C₂-C₈-alkenyl, —NH—C₂-C₈-alkynyl, —NH—C₃-C₁₂-cycloalkyl, —NH-aryl, —NH-heteroaryl, —NH-heterocycloalkyl, -dialkylamino, -diarylamino, -diheteroarylamino, —O—C₂-C₈-alkenyl, —O—C₂-C₈-alkynyl, —O—C₃-C₁₂-cycloalkyl, —O-aryl, —O-heteroaryl, —O-heterocycloalkyl, —C(O)—C₁-C₁₂-alkyl, —C(O)—C₂-C₈-alkenyl, —C(O)—C₂-C₈-alkynyl, —C(O)—C₃-C₁₂-cycloalkyl, —C(O)-aryl, —C(O)-heteroaryl, —C(O)-heterocycloalkyl, —CONH₂, —CONH—C₁-C₁₂-alkyl, —CONH—C₂-C₈-alkenyl, —CONH—C₂-C₈-alkynyl, —CONH—C₃-C₁₂-cycloalkyl, —CONH-aryl, —CONH-heteroaryl, —CONH-heterocycloalkyl, —OCO₂—C₁-C₁₂-alkyl, —OCO₂—C₂-C₈-alkenyl, —OCO₂—C₂-C₈-alkynyl, —OCO₂—C₃-C₁₂-cycloalkyl, —OCO₂-aryl, —OCO₂-heteroaryl, —OCO₂-heterocycloalkyl, —CO₂—C₁-C₁₂ alkyl, —CO₂—C₂-C₈ alkenyl, —CO₂—C₂-C₈ alkynyl, CO₂—C₃-C₁₂-cycloalkyl, —CO₂-aryl, CO₂-heteroaryl, CO₂-heterocyloalkyl, —OCONH₂, —OCONH—C₁-C₁₂-alkyl, —OCONH—C₂-C₈-alkenyl, —OCONH—C₂-C₈-alkynyl, —OCONH—C₃-C₁₂-cycloalkyl, —OCONH-aryl, —OCONH-heteroaryl, —OCONH-heterocyclo-alkyl, —NHC(O)H, —NHC(O)—C₁-C₁₂-alkyl, —NHC(O)—C₂—C₈-alkenyl, —NHC(O)—C₂-C₈-alkynyl, —NHC(O)—C₃-C₁₂-cycloalkyl, —NHC(O)-aryl, —NHC(O)— heteroaryl, —NHC(O)-heterocyclo-alkyl, —NHCO₂—C₁-C₁₂-alkyl, —NHCO₂—C₂-C₈-alkenyl, —NHCO₂—C₂-C₈-alkynyl, —NHCO₂—C₃-C₁₂-cycloalkyl, —NHCO₂-aryl, —NHCO₂-heteroaryl, —NHCO₂-heterocycloalkyl, —NHC(O)NH₂, —NHC(O)NH—C₁-C₁₂-alkyl, —NHC(O)NH—C₂-C₈-alkenyl, —NHC(O)NH—C₂-C₈-alkynyl, —NHC(O)NH—C₃-C₁₂-cycloalkyl, —NHC(O)NH-aryl, —NHC(O)NH-heteroaryl, —NHC(O)NH-heterocycloalkyl, NHC(S)NH₂, —NHC(S)NH—C₁-C₁₂-alkyl, —NHC(S)NH—C₂-C₈-alkenyl, —NHC(S)NH—C₂-C₈-alkynyl, —NHC(S)NH—C₃-C₁₂-cycloalkyl, —NHC(S)NH-aryl, —NHC(S)NH-heteroaryl, —NHC(S)NH-heterocycloalkyl, —NHC(NH)NH₂, —NHC(NH)NH—C₁-C₁₂-alkyl, —NHC(NH)NH—C₂-C₈-alkenyl, —NHC(NH)NH—C₂-C₈-alkynyl, —NHC(NH)NH—C₃-C₁₂-cycloalkyl, —NHC(NH)NH-aryl, —NHC(NH)NH-heteroaryl, —NHC(NH)NH-heterocycloalkyl, —NHC(NH)—C₁-C₁₂-alkyl, —NHC(NH)—C₂-C₈-alkenyl, —NHC(NH)—C₂-C₈-alkynyl, —NHC(NH)—C₃-C₁₂-cycloalkyl, —NHC(NH)-aryl, —NHC(NH)-heteroaryl, —NHC(NH)-heterocycloalkyl, —C(NH)NH—C₁-C₁₂-alkyl, —C(NH)NH—C₂-C₈-alkenyl, —C(NH)NH—C₂-C₈-alkynyl, —C(NH)NH—C₃-C₁₂-cycloalkyl, —C(NH)NH-aryl, —C(NH)NH-heteroaryl, —C(NH)NH-heterocycloalkyl, —S(O)—C₁-C₁₂-alkyl, —S(O)—C₂-C₈-alkenyl, —S(O)—C₂-C₈-alkynyl, —S(O)—C₃-C₁₂-cycloalkyl, —S(O)-aryl, —S(O)-heteroaryl, —S(O)— heterocycloalkyl, —SO₂NH₂, —SO₂NH—C₁-C₁₂-alkyl, —SO₂NH—C₂-C₈-alkenyl, —SO₂NH—C₂-C₈-alkynyl, —SO₂NH—C₃-C₁₂-cycloalkyl, —SO₂NH-aryl, —SO₂NH-heteroaryl, —SO₂NH-heterocycloalkyl, —NHSO₂—C₁-C₁₂-alkyl, —NHSO₂—C₂-C₈-alkenyl, —NHSO₂—C₂-C₈-alkynyl, —NHSO₂—C₃-C₁₂-cycloalkyl, —NHSO₂-aryl, —NHSO₂-heteroaryl, —NHSO₂-heterocycloalkyl, —CH₂NH₂, —CH₂SO₂CH₃, -aryl, -arylalkyl, -heteroaryl, -heteroarylalkyl, -heterocycloalkyl, —C₃-C₁₂-cycloalkyl, polyalkoxyalkyl, polyalkoxy, -methoxymethoxy, -methoxyethoxy, —SH, —S—C₁-C₁₂-alkyl, —S—C₂-C₈-alkenyl, —S—C₂-C₈-alkynyl, —S—C₃-C₁₂-cycloalkyl, —S-aryl, —S— heteroaryl, —S-heterocycloalkyl, or methylthio-methyl. It is understood that the aryls, heteroaryls, alkyls, cycloalkyls and the like can be further substituted.

The term “halo” or halogen” alone or as part of another substituent, as used herein, refers to a fluorine, chlorine, bromine, or iodine atom.

The term “optionally substituted”, as used herein, means that the referenced group may be substituted or unsubstituted. In one embodiment, the referenced group is optionally substituted with zero substituents, i.e., the referenced group is unsubstituted. In another embodiment, the referenced group is optionally substituted with one or more additional group(s) individually and independently selected from groups described herein.

The term “hydrogen” includes hydrogen and deuterium. In addition, the recitation of an atom includes other isotopes of that atom so long as the resulting compound is pharmaceutically acceptable.

The term “hydroxy activating group,” as used herein, refers to a labile chemical moiety which is known in the art to activate a hydroxyl group so that it will depart during synthetic procedures such as in a substitution or an elimination reaction. Examples of hydroxyl activating group include, but not limited to, mesylate, tosylate, triflate, p-nitrobenzoate, phosphonate and the like.

The term “activated hydroxyl,” as used herein, refers to a hydroxy group activated with a hydroxyl activating group, as defined above, including mesylate, tosylate, triflate, p-nitrobenzoate, phosphonate groups, for example.

The term “hydroxy protecting group,” as used herein, refers to a labile chemical moiety which is known in the art to protect a hydroxyl group against undesired reactions during synthetic procedures. After said synthetic procedure(s) the hydroxy protecting group as described herein may be selectively removed. Hydroxy protecting groups as known in the art are described generally in T. H. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, New York (1999). Examples of hydroxyl protecting groups include benzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, tert-butoxy-carbonyl, isopropoxycarbonyl, diphenylmethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, allyloxycarbonyl, acetyl, formyl, chloroacetyl, trifluoroacetyl, methoxyacetyl, phenoxyacetyl, benzoyl, methyl, t-butyl, 2,2,2-trichloroethyl, 2-trimethylsilyl ethyl, allyl, benzyl, triphenyl-methyl (trityl), methoxymethyl, methylthiomethyl, benzyloxymethyl, 2-(trimethylsilyl)-ethoxymethyl, methanesulfonyl, trimethylsilyl, triisopropylsilyl, and the like.

The term “protected hydroxy,” as used herein, refers to a hydroxy group protected with a hydroxy protecting group, as defined above, including benzoyl, acetyl, trimethylsilyl, triethylsilyl, methoxymethyl groups, for example.

The term “hydroxy prodrug group,” as used herein, refers to a promoiety group which is known in the art to change the physicochemical, and hence the biological properties of a parent drug in a transient manner by covering or masking the hydroxy group. After said synthetic procedure(s), the hydroxy prodrug group as described herein must be capable of reverting back to hydroxy group in vivo. Hydroxy prodrug groups as known in the art are described generally in Kenneth B. Sloan, Prodrugs, Topical and Ocular Drug Delivery, (Drugs and the Pharmaceutical Sciences; Volume 53), Marcel Dekker, Inc., New York (1992).

The term “amino protecting group,” as used herein, refers to a labile chemical moiety which is known in the art to protect an amino group against undesired reactions during synthetic procedures. After said synthetic procedure(s) the amino protecting group as described herein may be selectively removed. Amino protecting groups as known in the art are described generally in T. H. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, New York (1999). Examples of amino protecting groups include, but are not limited to, methoxycarbonyl, t-butoxycarbonyl, 9-fluorenyl-methoxycarbonyl, benzyloxycarbonyl, and the like.

The term “protected amino,” as used herein, refers to an amino group protected with an amino protecting group as defined above.

The term “leaving group” means a functional group or atom which can be displaced by another functional group or atom in a substitution reaction, such as a nucleophilic substitution reaction. By way of example, representative leaving groups include chloro, bromo and iodo groups; sulfonic ester groups, such as mesylate, tosylate, brosylate, nosylate and the like; and acyloxy groups, such as acetoxy, trifluoroacetoxy and the like.

The term “aprotic solvent,” as used herein, refers to a solvent that is relatively inert to proton activity, i.e., not acting as a proton-donor. Examples include, but are not limited to, hydrocarbons, such as hexane and toluene, for example, halogenated hydrocarbons, such as, for example, methylene chloride, ethylene chloride, chloroform, and the like, heterocyclic compounds, such as, for example, tetrahydrofuran and N-methylpyrrolidinone, and ethers such as diethyl ether, bis-methoxymethyl ether. Such compounds are well known to those skilled in the art, and it will be obvious to those skilled in the art that individual solvents or mixtures thereof may be preferred for specific compounds and reaction conditions, depending upon such factors as the solubility of reagents, reactivity of reagents and preferred temperature ranges, for example. Further discussions of aprotic solvents may be found in organic chemistry textbooks or in specialized monographs, for example: Organic Solvents Physical Properties and Methods of Purification, 4th ed., edited by John A. Riddick et al., Vol. II, in the Techniques of Chemistry Series, John Wiley & Sons, N Y, 1986.

The term “protic solvent,” as used herein, refers to a solvent that tends to provide protons, such as an alcohol, for example, methanol, ethanol, propanol, isopropanol, butanol, t-butanol, and the like. Such solvents are well known to those skilled in the art, and it will be obvious to those skilled in the art that individual solvents or mixtures thereof may be preferred for specific compounds and reaction conditions, depending upon such factors as the solubility of reagents, reactivity of reagents and preferred temperature ranges, for example. Further discussions of protogenic solvents may be found in organic chemistry textbooks or in specialized monographs, for example: Organic Solvents Physical Properties and Methods of Purification, 4th ed., edited by John A. Riddick et al., Vol. II, in the Techniques of Chemistry Series, John Wiley & Sons, N Y, 1986.

Combinations of substituents and variables envisioned by this invention are only those that result in the formation of stable compounds. The term “stable,” as used herein, refers to compounds which possess stability sufficient to allow manufacture and which maintains the integrity of the compound for a sufficient period of time to be useful for the purposes detailed herein (e.g., therapeutic or prophylactic administration to a subject).

The synthesized compounds can be separated from a reaction mixture and further purified by a method such as column chromatography, high pressure liquid chromatography, or recrystallization. As can be appreciated by the skilled artisan, further methods of synthesizing the compounds of the invention will be evident to those of ordinary skill in the art. Additionally, the various synthetic steps may be performed in an alternate sequence or order to give the desired compounds. Synthetic chemistry transformations and protecting group methodologies (protection and deprotection) useful in synthesizing the compounds described herein are known in the art and include, for example, those such as described in R. Larock, Comprehensive Organic Transformations, 2^(nd) Ed. Wiley-VCH (1999); T. W. Greene and P. G. M. Wuts, Protective Groups in Organic Synthesis, 3rd Ed., John Wiley and Sons (1999); L. Fieser and M. Fieser, Fieser and Fieser's Reagents for Organic Synthesis, John Wiley and Sons (1994); and L. Paquette, ed., Encyclopedia of Reagents for Organic Synthesis, John Wiley and Sons (1995), and subsequent editions thereof.

The term “subject,” as used herein, refers to an animal. Preferably, the animal is a mammal. More preferably, the mammal is a human. A subject also refers to, for example, dogs, cats, horses, cows, pigs, guinea pigs, fish, birds and the like.

The compounds of this invention may be modified by appending appropriate functionalities to enhance selective biological properties. Such modifications are known in the art and may include those which increase biological penetration into a given biological system (e.g., blood, lymphatic system, central nervous system), increase oral availability, increase solubility to allow administration by injection, alter metabolism and alter rate of excretion.

The compounds described herein contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-, or as (D)- or (L)- for amino acids. The present invention is meant to include all such possible isomers, as well as their racemic and optically pure forms. Optical isomers may be prepared from their respective optically active precursors by the procedures described above, or by resolving the racemic mixtures. The resolution can be carried out in the presence of a resolving agent, by chromatography or by repeated crystallization or by some combination of these techniques which are known to those skilled in the art. Further details regarding resolutions can be found in Jacques, et al., Enantiomers, Racemates, and Resolutions (John Wiley & Sons, 1981). When the compounds described herein contain olefinic double bonds, other unsaturation, or other centers of geometric asymmetry, and unless specified otherwise, it is intended that the compounds include both E and Z geometric isomers or cis- and trans-isomers. Likewise, all tautomeric forms are also intended to be included. Tautomers may be in cyclic or acyclic. The configuration of any carbon-carbon double bond appearing herein is selected for convenience only and is not intended to designate a particular configuration unless the text so states; thus a carbon-carbon double bond or carbon-heteroatom double bond depicted arbitrarily herein as trans may be cis, trans, or a mixture of the two in any proportion.

Certain compounds of the present invention may also exist in different stable conformational forms which may be separable. Torsional asymmetry due to restricted rotation about an asymmetric single bond, for example because of steric hindrance or ring strain, may permit separation of different conformers. The present invention includes each conformational isomer of these compounds and mixtures thereof.

As used herein, the term “pharmaceutically acceptable salt,” refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio. Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge, et al. describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 66: 1-19 (1977). The salts can be prepared in situ during the final isolation and purification of the compounds of the invention, or separately by reacting the free base function with a suitable organic acid. Examples of pharmaceutically acceptable salts include, but are not limited to, nontoxic acid addition salts are salts of an amino group formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid or by using other methods used in the art such as ion exchange. Other pharmaceutically acceptable salts include, but are not limited to, adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentane-propionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate, persulfate, 3-phenylpropionate, phosphate, picrate, pivalate, propionate, stearate, succinate, sulfate, tartrate, thiocyanate, p-toluenesulfonate, undecanoate, valerate salts, and the like. Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like. Further pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed using counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, alkyl having from 1 to 6 carbon atoms, sulfonate and aryl sulfonate.

As used herein, the term “pharmaceutically acceptable ester” refers to esters which hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Suitable ester groups include, for example, those derived from pharmaceutically acceptable aliphatic carboxylic acids, particularly alkanoic, alkenoic, cycloalkanoic and alkanedioic acids, in which each alkyl or alkenyl moiety advantageously has not more than 6 carbon atoms. Examples of particular esters include, but are not limited to, esters of C₁-C₆-alkanoic acids.

Pharmaceutical Compositions

The pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the present invention formulated together with one or more pharmaceutically acceptable carriers or excipients.

As used herein, the term “pharmaceutically acceptable carrier or excipient” means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols such as propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.

The pharmaceutical compositions of this invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir, preferably by oral administration or administration by injection. The pharmaceutical compositions of this invention may contain any conventional non-toxic pharmaceutically-acceptable carriers, adjuvants or vehicles. In some cases, the pH of the formulation may be adjusted with pharmaceutically acceptable acids, bases or buffers to enhance the stability of the formulated compound or its delivery form. The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intraarticular, intra-arterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.

Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions, may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectable.

The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.

In order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution, which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle. Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions that are compatible with body tissues.

Compositions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or: a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.

The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes.

Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulation, ear drops, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.

The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to the compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons.

Transdermal patches have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms can be made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.

For pulmonary delivery, a therapeutic composition of the invention is formulated and administered to the patient in solid or liquid particulate form by direct administration e.g., inhalation into the respiratory system. Solid or liquid particulate forms of the active compound prepared for practicing the present invention include particles of respirable size: that is, particles of a size sufficiently small to pass through the mouth and larynx upon inhalation and into the bronchi and alveoli of the lungs. Delivery of aerosolized therapeutics, particularly aerosolized antibiotics, is known in the art (see, for example U.S. Pat. No. 5,767,068 to Van Devanter et al., U.S. Pat. No. 5,508,269 to Smith et al., and WO 98/43650 by Montgomery, all of which are incorporated herein by reference).

Antiviral Activity

An inhibitory amount or dose of the compounds of the present invention may range from about 0.01 mg/Kg to about 500 mg/Kg, alternatively from about 1 to about 50 mg/Kg. Inhibitory amounts or doses will also vary depending on route of administration, as well as the possibility of co-usage with other agents.

According to the methods of treatment of the present invention, viral infections, conditions are treated or prevented in a patient such as a human or another animal by administering to the patient a therapeutically effective amount of a compound of the invention, in such amounts and for such time as is necessary to achieve the desired result.

By a “therapeutically effective amount” of a compound of the invention is meant an amount of the compound which confers a therapeutic effect on the treated subject, at a reasonable benefit/risk ratio applicable to any medical treatment. The therapeutic effect may be objective (i.e., measurable by some test or marker) or subjective (i.e., subject gives an indication of or feels an effect). An effective amount of the compound described above may range from about 0.1 mg/Kg to about 500 mg/Kg, preferably from about 1 to about 50 mg/Kg. Effective doses will also vary depending on route of administration, as well as the possibility of co-usage with other agents. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or contemporaneously with the specific compound employed; and like factors well known in the medical arts.

The total daily dose of the compounds of this invention administered to a human or other animal in single or in divided doses can be in amounts, for example, from 0.01 to 50 mg/kg body weight or more usually from 0.1 to 25 mg/kg body weight. Single dose compositions may contain such amounts or submultiples thereof to make up the daily dose.

In general, treatment regimens according to the present invention comprise administration to a patient in need of such treatment from about 10 mg to about 1000 mg of the compound(s) of this invention per day in single or multiple doses.

The compounds of the present invention described herein can, for example, be administered by injection, intravenously, intra-arterial, subdermally, intraperitoneally, intramuscularly, or subcutaneously; or orally, buccally, nasally, transmucosally, topically, in an ophthalmic preparation, or by inhalation, with a dosage ranging from about 0.1 to about 500 mg/kg of body weight, alternatively dosages between 1 mg and 1000 mg/dose, every 4 to 120 hours, or according to the requirements of the particular drug. The methods herein contemplate administration of an effective amount of compound or compound composition to achieve the desired or stated effect. Typically, the pharmaceutical compositions of this invention will be administered from about 1 to about 6 times per day or alternatively, as a continuous infusion. Such administration can be used as a chronic or acute therapy. The amount of active ingredient that may be combined with pharmaceutically excipients or carriers to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. A typical preparation will contain from about 5% to about 95% active compound (w/w). Alternatively, such preparations may contain from about 20% to about 80% active compound.

Lower or higher doses than those recited above may be required. Specific dosage and treatment regimens for any particular patient will depend upon a variety of factors, including the activity of the specific compound employed, the age, body weight, general health status, sex, diet, time of administration, rate of excretion, drug combination, the severity and course of the disease, condition or symptoms, the patient's disposition to the disease, condition or symptoms, and the judgment of the treating physician.

Upon improvement of a patient's condition, a maintenance dose of a compound, composition or combination of this invention may be administered, if necessary. Subsequently, the dosage or frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained when the symptoms have been alleviated to the desired level. Patients may, however, require intermittent treatment on a long-term basis upon any recurrence of disease symptoms.

When the compositions of this invention comprise a combination of a compound of the Formula described herein and one or more additional therapeutic or prophylactic agents, both the compound and the additional agent should be present at dosage levels of between about 1 to 100%, and more preferably between about 5 to 95% of the dosage normally administered in a monotherapy regimen. The additional agents may be administered separately, as part of a multiple dose regimen, from the compounds of this invention. Alternatively, those agents may be part of a single dosage form, mixed together with the compounds of this invention in a single composition.

The said “additional therapeutic or prophylactic agents” includes but not limited to, immune therapies (e.g. interferon), therapeutic vaccines, antifibrotic agents, anti-inflammatory agents such as corticosteroids or NSAIDs, bronchodilators such as beta-2 adrenergic agonists and xanthines (e.g. theophylline), mucolytic agents, anti-muscarinics, anti-leukotrienes, inhibitors of cell adhesion (e.g. ICAM antagonists), anti-oxidants (e.g. N-acetylcysteine), cytokine agonists, cytokine antagonists, lung surfactants and/or antimicrobial and anti-viral agents (e.g. ribavirin and amantidine). The compositions according to the invention may also be used in combination with gene replacement therapy.

Combination and Alternation Therapy for HBV

It has been recognized that drug-resistant variants of HIV, HBV and HCV can emerge after prolonged treatment with an antiviral agent. Drug resistance most typically occurs by mutation of a gene that encodes for a protein such as an enzyme used in viral replication, and most typically in the case of HIV, reverse transcriptase, protease, or DNA polymerase, and in the case of HBV, DNA polymerase, or in the case of HCV, RNA polymerase, protease, or helicase. Recently, it has been demonstrated that the efficacy of a drug against HIV infection can be prolonged, augmented, or restored by administering the compound in combination or alternation with a second, and perhaps third, antiviral compound that induces a different mutation from that caused by the principle drug. The compounds can be used for combination are selected from the group consisting of a HBV polymerase inhibitor, interferon, TLR modulators such as TLR-7 agonists or TLR-9 agonists, therapeutic vaccines, immune activator of certain cellular viral RNA sensors, viral entry inhibitor, viral maturation inhibitor, distinct capsid assembly modulator, antiviral compounds of distinct or unknown mechanism, and combination thereof. Alternatively, the pharmacokinetics, biodistribution, or other parameter of the drug can be altered by such combination or alternation therapy. In general, combination therapy is typically preferred over alternation therapy because it induces multiple simultaneous stresses on the virus.

Preferred compounds for combination or alternation therapy for the treatment of HBV include 3TC, FTC, L-FMAU, interferon, adefovir dipivoxil, entecavir, telbivudine (L-dT), valtorcitabine (3′-valinyl L-dC), β-D-dioxolanyl-guanine (DXG), β-D-dioxolanyl-2,6-diaminopurine (DAPD), and β-D-dioxolanyl-6-chloropurine (ACP), famciclovir, penciclovir, lobucavir, ganciclovir, and ribavirin.

Although the invention has been described with respect to various preferred embodiments, it is not intended to be limited thereto, but rather those skilled in the art will recognize that variations and modifications may be made therein which are within the spirit of the invention and the scope of the appended claims.

Abbreviations

Abbreviations which may be used in the descriptions of the scheme and the examples that follow are: Ac for acetyl; AcOH for acetic acid; AIBN for azobisisobutyronitrile; BINAP for 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl; Boc₂O for di-tert-butyl-dicarbonate; Boc for t-butoxycarbonyl; Bpoc for 1-methyl-1-(4-biphenylyl)ethyl carbonyl; Bz for benzoyl; Bn for benzyl; BocNHOH for tert-butyl N-hydroxycarbamate; t-BuOK for potassium tert-butoxide; Bu₃SnH for tributyltin hydride; BOP for (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium Hexafluorophosphate; Brine for sodium chloride solution in water; BSA for N,O-bis(trimethylsilyl)acetamide; CDI for carbonyldiimidazole; CH₂Cl₂ for dichloromethane; CH₃ for methyl; CH₃CN for acetonitrile; Cs₂CO₃ for cesium carbonate; CuCl for copper (I) chloride; CuI for copper (I) iodide; dba for dibenzylidene acetone; dppb for diphenylphos-phinobutane; DBU for 1,8-diazabicyclo[5.4.0]-undec-7-ene; DCC for N,N′-dicyclohexyl-carbodiimide; DEAD for diethylazodicarboxylate; DIAD for diisopropyl azodicarboxylate; DIPEA or (i-Pr)₂EtN for N,N,-diisopropylethyl amine; Dess-Martin periodinane for 1,1,1-tris(acetyloxy)-1,1-dihydro-1,2-benziodoxol-3-(1H)-one; DMAP for 4-dimethylamino-pyridine; DME for 1,2-dimethoxyethane; DMF for N,N-dimethylformamide; DMSO for dimethyl sulfoxide; DMT for di(methoxyphenyl)-phenylmethyl or dimethoxytrityl; DPPA for diphenylphosphoryl azide; EDC for N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide; EDC HCl for N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride; EtOAc for ethyl acetate; EtOH for ethanol; Et₂O for diethyl ether; HATU for O-(7-azabenzotriazol-1-yl)-N,N,N′,N′,-tetramethyluronium Hexafluoro-phosphate; HCl for hydrogen chloride; HOBT for 1-hydroxybenzotriazole; K₂CO₃ for potassium carbonate; n-BuLi for n-butyl lithium; i-BuLi for i-butyl lithium; t-BuLi for t-butyl lithium; PhLi for phenyl lithium; LDA for lithium diisopropylamide; LiTMP for lithium 2,2,6,6-tetramethyl-piperidinate; MeOH for methanol; Mg for magnesium; MOM for methoxymethyl; Ms for mesyl or —SO₂—CH₃; Ms₂O for methanesulfonic anhydride or mesyl-anhydride; MTBE for t-butyl methyl ether; NaN(TMS)₂ for sodium bis(trimethylsilyl)amide; NaCl for sodium chloride; NaH for sodium hydride; NaHCO₃ for sodium bicarbonate or sodium hydrogen carbonate; Na₂CO₃ sodium carbonate; NaOH for sodium hydroxide; Na₂SO₄ for sodium sulfate; NaHSO₃ for sodium bisulfite or sodium hydrogen sulfite; Na₂S₂O₃ for sodium thiosulfate; NH₂NH₂ for hydrazine; NH₄HCO₃ for ammonium bicarbonate; NH₄Cl for ammonium chloride; NMO for N-methylmorpholine N-oxide; NaIO₄ for sodium periodate; Ni for nickel; OH for hydroxyl; OsO₄ for osmium tetroxide; PTSA for p-toluenesulfonic acid; PPTS for pyridiniump-toluenesulfonate; TBAF for tetrabutylammonium fluoride; TEA or Et₃N for triethylamine; TES for triethylsilyl; TESCl for triethylsilyl chloride; TESOTf for triethylsilyl trifluoromethanesulfonate; TFA for trifluoroacetic acid; THF for tetrahydrofuran; TMEDA for N,N,N′,N′-tetramethylethylene-diamine; TPP or PPh₃ for triphenyl-phosphine; Troc for 2,2,2-trichloroethyl carbonyl; Ts for tosyl or —SO₂—C₆H₄CH₃; Ts₂O for tolylsulfonic anhydride or tosyl-anhydride; TsOH for p-tolylsulfonic acid; Pd for palladium; Ph for phenyl; POPd for dihydrogen dichlorobis(di-tert-butylphosphinito-KP)palladate(II); Pd₂(dba)₃ for tris(dibenzylideneacetone) dipalladium (O); Pd(PPh₃)₄ for tetrakis(triphenylphosphine)palladium (O); PdCl₂(PPh₃)₂ for trans-dichlorobis-(triphenylphosphine)palladium (II); Pt for platinum; Rh for rhodium; rt for room temperature; Ru for ruthenium; TBS for tert-butyl dimethylsilyl; TMS for trimethylsilyl; or TMSCl for trimethylsilyl chloride; DCM for dichloromethane; and PMB for 4-methyoxylbenzyl.

Synthetic Methods

The compounds and processes of the present invention will be better understood in connection with the following synthetic schemes that illustrate the methods by which the compounds of the invention may be prepared. These schemes are of illustrative purpose, and are not meant to limit the scope of the invention. Equivalent, similar, or suitable solvents, reagents or reaction conditions may be substituted for those particular solvents, reagents, or reaction conditions described herein without departing from the general scope of the method of synthesis.

The compounds of the present invention may be prepared via several different synthetic strategies and routes from a variety of phenyl, 5- and 6-membered heteroaryl or fused bicyclic aryl or heteroaryl precursors using the reactions that are known to those skilled in the art. In a general strategy, specific aryl or heteroaryl moieties in the target molecules are connected together via suitable reactions from properly functionalized aryl or heteroaryl precursors. These reactions include, but not limited to, organometallics catalyzed cross-coupling, amino nucleophilic displacement reaction, carbodiimide (DCC, EDC) mediated amide formation, Curtius rearrangement, et al. More specifically, two general strategies could be envisioned; in the first scenario, the amino group of Y already exists in optionally functionalized Y, through it Y is connected to X via A (or directly when A is absent) or to Z through proper coupling reactions. In the other scenario, the amino group in Y is surrogated with other functional groups such as carboxyl acid, halo, tiflate, methylthioly, and so on. The amino group in Y was produced when the aryl or the hetreoaryl group in Y is connected to X via A (or directly when A is absent) or Z through proper functional group manipulation.

As illustrated in Scheme 1, wherein X, A, Y, L, R₁ are as defined previously for formula I; LG₁ is hydrogen, carboxyl acid, ester, halo, methylthio, triflate; LG₂ is independently selected from OH, halo; LG₃ is amino, halo, and A-LG₄ wherein A is azole; LG₄ is halo, amino, boronic acid/ester, organotin or organozinc moiety. An optionally substituted aryl or heteroaryl 1-1 reacts with 1-2 to give an intermediate 1-3 in which the amino in Y was connected with Z. In most case, this intermediate is very active and was used directly to reacts with 1-4 (wherein L is an amine moiety) by a nucleophilic displacement to afford advanced intermediate 1-5. This intermediate 1-5 then reacts with an optionally substituted 1-6 to afford a compound of Formula (I) via an amide formation reaction (mediated by EDC, or HATU). When A is azole, a reaction is a palladium catalyzed coupling condition of Suzuki, Stille, Negishi or the like known to those skilled in the art. Alternatively, the starting material 1-1 could reacts with 1-6 to give the advanced intermediate 1-3′ in which the amino in Y is connected to A (X when A is absent). The reactions employed here include, but not limited to, urea formation, palladium catalyzed amination. When 1-3′ reacted with 1-2 in the presence of a proper base such as pyridine or TEA will afford active intermediate 1-5′ which subsequently reacts with 1-4 to afford a compound of Formula (I). Additionally, when Z is CO, intermediate 1-3′ may be converted to a compound of Formula (I) via palladium catalyzed carbonylation/amination sequence in one operation. Again additionally, when Z is SO₂, intermediate 1-5′ may obtained from 1-3′ via a two-step procedure; first 1-5′ reacts with (4-methoxylphenyl)methanethiol (PMBSH) in the presence of a palladium catalyst to offer a thio intermediate followed by oxidation with trichloroisocyanuric acid or 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione. It should be appreciated that the chemistry just described above may be variable to switch the coupling partners at certain steps to afford the same or isomeric target molecule.

As a specific example shown in Scheme 1a, azolylamino compound 1-1a was treated with phosgene to afford an intermediate which sequentially reacts with an amine to give 1-3a. The ester functional group in 1-3a is hydrolyzed to the carboxyl acid when exposed to a suitable base such as LiOH, NaOH in protonic solvent (H₂O, EtOH). The carboxyl acid reacts with an arylamino compound in the present of a suitable dehydrating reagent such as EDC, HATU and an organic base (TEA, DIPEA) in proper organic solvent (CH₂Cl₂, CH₃CN, DMF) to give a compound with general formula Ia.

As illustrated in Scheme 2, wherein X, A, Y, L, R₁, LG₁, LG₂ and LG₃ are as defined previously. Y′ is the aryl or heteroaryl core of Y. L₁ is carboxyl acid, halo and behaves as a surrogate group for amino of Y. An optionally substituted 2-1 reacts with an optionally substituted 2-2 to give the advanced intermediate 1-3 in which the amino in Y is generated and connected with Z. The proper reaction employed here includes, but not limited to, Curtius reaction, amino nucleophilic displacement, palladium catalyzed amination and so on. Follow similar procedure as in Scheme 1, a compound with general formula I will be obtained. Alternatively, the starting material 2-1 reacts with 1-6 to give the advanced intermediate 1-3′ in which the amino in Y is generated and connected to A (X when A is absent). The reactions employed here include, but not limited to, Curtius reaction, amino nucleophilic displacement, palladium catalyzed amination and so on. Following similar procedure as in Scheme 1, a compound with general formula I also will be obtained. It should be appreciated that the chemistry just described above may be variable to switch the coupling partners at certain steps to afford the same or isomeric target molecule.

A specific example is shown in Scheme 2a. An azolybromide 2-1a may react with PMBSH in the presence of a proper palladium catalyst to afford a benzylthio intermediate. When this intermediate is oxidized with trichloroisocyanuric acid, a sulfonyl chloride will be produced. This sulfonyl chloride when is treated with an amine in the presence of a proper organic base, such as pyridine, will afford an advanced intermediate 2-2a. The ester functional group in 2-2a is converted to a carboxyl acid via saponification with LiOH in protonic solvent such as EtOH. When this carboxyl acid is reacted with DPPA and an arylamine via Curtius reaction, a compound with general formula Ib shall be obtained.

Another specific example is shown in Scheme 2b. An indazole 2-1a is reacted with chlorosulfonic acid to afford a sulfonyl chloride regio-specifically. This sulfonyl chloride is reacted with an amine in the presence of a suitable organic base such as pyridine or TEA to provide an intermediate 2-2b. When this intermediate is reacted with an arylamine, via either direct displacement or optionally catalyzed by a palladium complex will afford a compound with general structure Ic.

It will be appreciated that, with appropriate manipulation and protection of any chemical functionality, synthesis of compounds of Formula (I) is accomplished by methods analogous to those above and to those described in the Experimental section. Suitable protecting groups can be found, but are not restricted to, those found in T W Greene and P G M Wuts “Protective Groups in Organic Synthesis”, 3rd Ed (1999), J Wiley and Sons.

All references cited herein, whether in print, electronic, computer readable storage media or other form, are expressly incorporated by reference in their entirety, including but not limited to, abstracts, articles, journals, publications, texts, treatises, internet web sites, databases, patents, and patent publications.

Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art and such changes and modifications including, without limitation, those relating to the chemical structures, substituents, derivatives, formulations and/or methods of the invention may be made without departing from the spirit of the invention and the scope of the appended claims.

Although the invention has been described with respect to various preferred embodiments, it is not intended to be limited thereto, but rather those skilled in the art will recognize that variations and modifications may be made therein which are within the spirit of the invention and the scope of the appended claims.

EXAMPLES

The compounds and processes of the present invention will be better understood in connection with the following examples, which are intended as an illustration only and not limiting of the scope of the invention. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art and such changes and modifications including, without limitation, those relating to the chemical structures, substituents, derivatives, formulations and/or methods of the invention may be made without departing from the spirit of the invention and the scope of the appended claims.

Although the invention has been described with respect to various preferred embodiments, it is not intended to be limited thereto, but rather those skilled in the art will recognize that variations and modifications may be made therein which are within the spirit of the invention and the scope of the appended claims.

Example 1

Step 1a. To a suspension of 6-chloro-1H-indazole (3.0 g, 19.66 mmol) in 2M NaOH (70 mL) was added a solution of Bra (2.32 g, 14.52 mmol) in 2M NaOH (30 mL) drop wise. The mixture was stirred for 1.5 hours at rt. The pH value of the solution was adjusted to 8 with 3M HCl and partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (3.4 g, 44%). ESI-MS m/z=231.00, 233.00 [M+H]⁺.

Step 1b. A mixture of the compound from step 1a (2.0 g, 8.64 mmol) in chlorosulfuric acid (15 mL) was stirred for 14 hours at 100° C. After being cooled to rt, the reaction was poured into ice water slowly. The solids were collected by filtration; washed with water and dried in vacuum to give the desired compound (2.1 g, 74%) as a yellow solid, which was used directly in the next step without further purification.

Step 1c. A solution of the compound from step 1b (1.98 g, 6.0 mmol), 4-[(tert butyldimethylsilyl)oxy]piperidine (1.29 g, 5.99 mmol) and Pyridine (1.42 g, 17.98 mmol) in CH₂Cl₂ (50 mL) was stirred for 3 hours at rt. The solution was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (1.0 g, 33%). ESI-MS m/z=508.05, 510.05 [M+H]⁺.

Step 1d. A mixture of the compound from step 1c (750 mg, 1.47 mmol), 3,4,5-trifluoroaniline (238 mg, 1.62 mmol), Pd₂(dba)₃ (135 mg, 0.14 mmol), Xantphos (85 mg, 0.14 mmol), Cs₂CO₃ (960 mg, 2.94 mmol) in 1,4-dioxane (10 mL) was irradiated with microwave radiation for 1 hour at 130° C. The solution was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (270 mg, 32%). ESI-MS m/z=575.25, 577.25 [M+H]⁺.

Step 1e. A solution of the compound from step 1d (150 mg, 0.26 mmol) and TFA (5 mL) in DCM (5 mL) was stirred for 1 hour at rt before was concentrated. The residue was chromatographed (silica, petroleum ether-ethyl acetate) to give the title compound as a white solid. (45 mg, 38%). ESI-MS m/z=461.0, 462.9 [M+H]⁺.

Example 2

Step 2a. To a solution of ethyl 5-bromo-1-methyl-1H-pyrazole-3-carboxylate (500 mg, 2.15 mmol) in dioxane (10 mL) was added Pd₂(dba)₃ (450 mg, 0.44 mmol), Xantphos (250 mg, 0.43 mmol), DIPEA (550 mg, 4.26 mmol), (4-methoxylphenyl)methanethiol (300 mg, 2.40 mmol) under N₂ atmosphere and stirred for 3 hour at 110° C. The mixture was cooled to r.t and quenched by water and partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound (550 mg, 84%) as yellow oil. ESI-MS m/z=278.09 [M+H]⁺.

Step 2b. A solution of compound form step 2a (400 mg, 1.44 mmol), 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione (700 mg, 3.14 mmol) in MeCN/AcOH/water 15 ml (80/3/2) was stirred for 1 hour at −5° C. before was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated to give the desired compound (500 mg) as a yellow oil. ESI-MS m/z=253.00 [M+H]⁺. This material was used directly in the next step without further purification.

Step 2c. A solution of compound form step 2b (500 mg, 1.98 mmol), 4-(tert-butyldimethyl-silyloxy)piperidine (375 mg, 1.74 mmol) in Pyridine (10 ml) was stirred for 4 hours at rt. The mixture was quenched by water and partitioned (EtOAc-brine), the organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed to give the desired compound as a yellow solid (400 mg, 47% for two steps). ESI-MS m/z=432.19 [M+H]⁺.

Step 2d. To a solution of compound form step 2c (400 mg, 0.93 mmol) in MeOH/H₂O (4:1, 15 mL), was added LiOH (89 mg, 3.70 mmol) at 0° C. The solution was stirred for 1 hour at rt before was adjusted to PH=5 with HCl (1M) and partitioned (EtOAc-brine). The organic layer was dried (Na₂SO₄), filtered and concentrated to give the desired product as a yellow solid (320 mg, 85%). ESI-MS m/z=404.16 [M+H]⁺. This material was used directly in the next step without further purification.

Step 2e. To a solution of compound form step 2d (300 mg, 0.74 mmol) in toluene (10 mL) was added 3,4,5-trifluorobenzenamine (132 mg, 0.89 mmol), DPPA (248 mg, 0.90 mmol) and Et₃N (150 mg, 1.49 mmol). The mixture was stirred for 4 hours at 80° C. cooled and partitioned (EtOAc-brine). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as an off-white solid (180 mg, 44%). ESI-MS m/z=548.19 [M+H]⁺.

Step 2f. A solution of compound form step 2e (180 mg, 0.33 mmol) in TFA (5 mL) was stirred for 30 minutes at rt before was concentrated and partitioned (EtOAc-brine). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the title compound as a white solid (51.5 mg, 36%) ESI-MS m/z=434.10 [M+H]⁺.

Example 3

Step 3a. A mixture of the triphosgene (5.25 g, 5.89 mmol), ethyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate (2.0 g, 11.82 mmol), TEA (4.77 g, 47.14 mmol) and piperidin-4-ol (1.79 g, 17.70 mmol) in DCM (50 mL) was stirred for 14 hours at 40° C. before it was concentrated and partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (2.8 g, 80%). ESI-MS m/z=297.25 [M+H]⁺. Step 3b. A solution of the compound from step 3a (500 mg, 1.69 mmol) and LiOH (162 mg, 6.76 mmol) in the mixture of THF:H₂O (5 mL) was stirred for 2 hours at rt. The pH of the solution was adjusted to 5 with HCl (2 M). The mixture was filtered to give the desired compound as white solid (240 mg, 53%). ESI-MS m/z=269.20 [M+H]⁺. Step 3c. A solution of the compound from step 3b (200 mg, 0.74 mmol), 3,4,5-trifluoroaniline (130 mg, 0.89 mmol), HATU (425 mg, 1.12 mmol) and DIPEA (240 mg, 1.86 mmol) in DMF (2 mL) was stirred for 2 hours at rt before was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the title compound as a white solid (50 mg, 17%). ESI-MS m/z=398.05 [M+H]⁺.

Example 4

Step 4a. A solution of 2-amino-4-chlorophenol (20.0 g, 14 mmol), KOH (2.4 g, 42 mmol), CS₂ (10.6 g 140 mmol) in EtOH (50 mL) was refluxed for 4 h. After concentrated, the residue was diluted with water (100 mL), acidified with HCl (2 M), extracted with DCM (2×250 mL). The organic phase was dried (Na₂SO₄) and concentrated to give the desired compound as brown solid (1.8 g, 72%). ESI-MS m/z=186.10, 188.10 [M+H]⁺. This material was used directly in the next step without further purification.

Step 4b. A mixture of compound from step 4a (1.6 g, 8.6 mmol), MeI (1.8 g, 12.9 mmol) and K₂CO₃ in DMF (20 mL) was stirred for 5 hours at 50° C. before was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated to give the desired compound (1.2 g, 70%) as a yellow oil. ESI-MS m/z=199.90, 201.90 [M+H]⁺. This material was used directly in the next step without further purification.

Step 4c. Compound form step 4b (1.1 g, 5.5 mmol) was added slowly to sulfurochloridic acid (10 mL) at 0° C. The mixture was stirred for 5 hours at 130° C. After cooled, the mixture was poured into ice H₂O slowly and partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated to give the desired compound as a yellow solid (650 mg, 40%). ESI-MS m/z=297.9, 299.9 [M+H]⁺. This material was used directly without further purification.

Step 4d. A solution of compound form step 4c (500 mg, 1.70 mmol), 4-(tert-butyldimethyl-silyloxy)piperidine (438.6 mg 2.04 mmol), Et₃N (343.4 mg, 3.4 mmol) in DCM (5 mL) was stirred for 2 hour at rt before was partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleumether) to give the desired product as a yellow solid (320 mg, 85%). ESI-MS m/z=477.25, 479.25 [M+H]⁺.

Step 4e. A mixture of compound form step 4d (200 mg, 0.42 mmol), 3,4,5-trifluorobenzenamine (61.7 mg 0.42 mmol) and Cs₂CO₃ (273.8 mg, 0.84 mmol) in DMF (5 mL) was stirred overnight at 70° C. After cooled, the mixture was partitioned (EtOAc-brine). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as an off-white solid (180 mg, 74%). ESI-MS m/z=576.30, 578.30 [M+H]⁺.

Step 4f. A solution of compound form step 4e (160 mg, 0.28 mmol) in DCM (1 mL) and TFA (1 mL) was stirred for 2 hours at 0° C. After concentrated, the residue was partitioned (EtOAc-brine). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the title compound as a white solid (50.9 mg, 39.7%). ESI-MS m/z=462.20, 464.20 [M+H]⁺.

Example 5

Step 5a. A mixture of tert-butyl 4-hydroxypiperidine-1-carboxylate (3.0 g, 14.9 mmol), NaH (1.6 g, 14.9 mmol) in THF (100 mL) was stirred for 1 hour at 0° C. Benzyl bromide (2.8 g, 16.4 mmol) in THF (10 mL) was added and stirred for 5 hours at 70° C. After cooled, the reaction was quenched with H₂O (200 mL) at 0° C. and partitioned (EtOAc-brine). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as yellow oil (3.3 g, 76.7%). ESI-MS m/z=192[M−Boc+H]⁺.

Step 5b. A solution of the compound from step 5a (3.0 g, 10.3 mmol) in DCM (20 mL) and TFA (10 mL) was stirred for 30 minutes at rt. It was concentrated to give the desired compound (3.0 g, 100%) as TFA salt and was used in next step without further purification. Step 5c. To the solution of the compound from step 5b (2.5 g, 8.7 mmol) and Et₃N (2.6 g, 26.1 mmol) in DCM (100 mL) was added sulfurochloridic acid (1.3 g, 11.3 mmol) dropwise at 0° C. The mixture was stirred overnight at rt before was diluted with DCM (100 mL) and washed with aq NH₄Cl and brine. The organic was dried (Na₂SO₄), filtered and concentrated. The residue was purified by Flash-Prep-HPLC ((IntelFlash-1): Column, C18; mobile phase, MeCN/H₂O, Detector, UV 220 nm) to give the desired compound as a yellow oil (1.5 g, 60%). ESI-MS m/z=270 [M−H]⁻.

Step 5d. The mixture of compound from step 5c (1.3 g, 4.8 mmol) and PCl₅ (1.0 g, 4.8 mmol) in toluene (100 mL) was stirred for 2 hours at 100° C. After cooled, it was concentrated, diluted with water and partitioned (CH₂Cl₂—H₂O). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (1.0 g, 71%). ¹H-NMR (300 MHz, DMSO-d6, 6, ppm): 1.74-2.14 (4H, m), 3.11-3.59 (4H, m), 3.70 (1H, tt), 4.54 (2H, d), 7.26-7.41 (5H, m).

Step 5e. A solution of the compound from step 5d (800 mg, 2.7 mmol), DMAP (848 mg, 6.9 mmol) and ethyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate (456 mg, 2.7 mmol) in DMF (6 mL) was stirred for 1 hour at rt and overnight at 60° C. It was diluted with DCM (100 mL), washed with aq NH₄Cl and brine. The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a yellow solid (230 mg, 25%). ESI-MS m/z=423 [M+H]⁺. Step 5f. To a solution of the compound from step 5e (230 mg, 0.55 mmol) in THF (3 ml) and water (3 ml) was added LiOH.H₂O (69.3 mg, 1.65 mmol). The reaction was stirred at rt for 2 hours before was acidified to PH=5 by HCl (1M) and partitioned (CH₂Cl₂—H₂O). The organic was dried (Na₂SO₄), filtered and concentrated to give the desired compound as white solid (180 mg, 83%). ESI-MS m/z=395.25 [M+H]⁺. Step 5g. The mixture of the compound from step 5f (180 mg, 0.45 mmol), 3,4,5-trifluorobenzenamine (66 mg, 0.45 mmol), HATU (171 mg, 0.45 mmol) and DIPEA (116 mg, 0.90 mmol) in DMF (5 mL) was stirred for overnight at rt. The mixture was partitioned (CH₂Cl₂—H₂O). The organic was dried (Na₂SO₄), filtered and concentrated. The residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as a white solid (87 mg, 37%). ESI-MS m/z=524 [M+H]⁺.

Step 5h. A mixture of the compound from step 5g (87 mg, 0.13 mmol) and palladium on carbon (10 wt %, 20 mg) in MeOH (7 mL) was stirred under H₂ (1 atm) at rt for 1 hour. The mixture was filtered and concentrated. The residue was purified by Flash-Prep-HPLC (IntelFlash-1): Column, C18; mobile phase, MeCN/H₂O, Detector, UV 220 nm) to give the desired compound as a white solid (11 mg, 20%). ESI-MS m/z=434 [M+H]⁺.

Example 6

Step 6a. A solution of ethyl 1-methyl-1H-imidazole-2-carboxylate (2.0 g, 13 mmol) in 8 ml conc. H₂SO₄ and 8 ml conc. HNO₃ was stirred for 3 hours at 70° C. The solution was diluted with H₂O, then adjusted to pH 7-8 with aq Na₂CO₃ solution and extracted with DCM. The organic layer was concentrated and chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as yellow solid (0.9 g, 34.7%). ESI-MS m/z=200.20 [M+H]⁺

Step 6b. A mixture of compound from step 6a (500 mg, 2.5 mmol), Fe (562 mg, 10 mmol) and NH₄Cl (672 mg, 12.5 mmol) in H₂O/EtOH (3 mL/3 mL) was stirred for 2 hours at 70° C. The mixture was cooled to rt and filtered. The filtrate was concentrated. The residue was partitioned (EtOAc-H₂O). The organic layer was dried over Na₂SO₄, concentrated and chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as orange solid (220 mg, 52.1%). ESI-MS m/z=170.00 [M+H]^(P) Step 6c. A solution of compound from step 6b (180 mg, 1.1 mmol), triphosgene (228 mg, 0.77 mmol), TEA (333 mg, 3.3 mmol) in DCM (12 mL) was stirred for 30 minutes at −78° C. 4-hydroxypiperidine (222 mg, 2.2 mmol) was added into the above solution. The mixture was stirred for 30 minutes at room temperature. It was concentrated and the residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as yellow solid (220 mg, 67.7%). ESI-MS m/z=297.15 [M+H]⁺

Step 6d A solution of compound from step 6c (220 mg, 0.74 mmol), LiOH (71 mg, 2.97 mmol) in THF/H₂O (6 mL/3 mL) was stirred for 40 minutes under N₂ atmosphere. It was concentrated and adjusted to pH=5 by 1 N HCl. It was filtered and dried in vacuum to give the desired compound as white solid (150 mg, 75.8%). ESI-MS m/z=269.15 [M+H]⁺ LC-MS-PH-ETA-B-109-4: (ES, m/z): [M+H]⁺=269.15 Step 6e. A solution of compound from step 4 (100 mg, 0.37 mmol), compound 2 (66 mg, 0.45 mmol), HATU (171 mg, 0.45 mmol), DIPEA (143 mg, 1.1 mmol) in DMF (2 mL) was stirred overnight at room temperature. The mixture was purified by Prep-HPLC (MeCN/H₂O, 01% FA) to give the title compound as white solid (70 mg, 47.6%). ESI-MS m/z=398.30 [M+H]⁺.

Example 7

Step 7a. To a solution of methyl 3-amino-4-chlorobenzoate (500 mg, 2.69 mmol) in CH₂Cl₂ (25 mL) at 0° C. was added triphosgene (959 mg, 13.02 mmol), triethylamine (3.26 g, 32.28 mmol) and piperidin-4-ol (300 mg, 2.96 mmol), and the resulting solution was stirred at 0° C. for 3 hours The solution was diluted with ethyl acetate and washed with brine. The organic was dried (Na₂SO₄) filtered and concentrated. The residue was chromatographed (silica, petroleum ether-ethyl acetate) to give the desired compound as yellow oil (620 mg, 73%). ESI-MS m/z=313.00, 315.00 [M+H]⁺. Step 7b. A mixture of the compound from step 7a (570 mg, 1.83 mmol) and LiOH (384 mg, 9.13 mmol) in H₂O (2 mL), THF (2 mL) was stirred for 2 hours at rt. The solution was adjusted to pH value at 4 and then extracted with EtOAc. The solution was dried over Na₂SO₄. The filtrate was concentrated to give the desired compound (430 mg, 79%) as white solids, which was used directly in the next step. ESI-MS m/z=299.20, 301.20 [M+H]⁺. Step 7c. A solution of the compounds from step 7b (150 mg, 0.50 mmol), 3,4,5-trifluorobenzenamine (89 mg, 0.60 mmol), HATU (285 mg, 0.75 mmol) and TEA (151 mg, 1.50 mmol) in DMF (5 mL) was stirred for 14 hours at rt. The solution was diluted with EtOAc, and washed with NaHCO₃(aq) and brine. The residue was chromatographed (silica, petroleum ether-ethyl acetate) to give the title compound as yellow solid (80 mg, 37%). ESI-MS m/z=428.10, 430.10 [M+H]⁺.

Example 8

Step 8a. To a stirred solution of the compound from Step 3a (130 mg, 0.44 mmol) in DCM (2.0 mL) was added imidazole (90 mg, 1.32 mmol), DMAP (11 mg, 0.09 mmol), and TBSCl (80 mg, 0.53 mmol) at 0° C. The resulting mixture was stirred at rt overnight. The reaction was quenched by addition of aqueous solution of NaHCO₃ (10 mL), and the mixture was extracted with DCM. The organic layers were combined, dried (Na₂SO₄) and concentrated to provide a crude product, which was purified by flash chromatography to give the desired product (165 mg, 91%). ESI-MS m/z=411.24 [M+H]⁺.

Step 8b. To a stirred solution of the compound from Step 8a (70 mg, 0.17 mmol) in EtOH (2.0 mL) was added a solution of 0.5 M LiOH (0.5 mL) at 0° C. The resulting mixture was stirred at rt for 2 hours. The mixture was diluted with water (5.0 mL), aq. HCl (1.0 M) was added to adjust the pH=−3, the resulting mixture was extracted with EtOAc (10 mL×3). The organic layers were combined, dried (Na₂SO₄) and concentrated to provide a crude product, which was used for next step reaction directly without any further purification. ESI-MS m/z=383.21 [M+H]⁺.

Step 8c. To stirred solution of the compound from Step 8b (38 mg, 0.10 mmol) in DMF (2.0 mL) was added DIPEA (19.4 mg, 0.15 mmol), 2-bromo-1-(3,4,5-trifluorophenyl)ethan-1-one (38.0 mg, 0.15 mmol) at 0° C. The resulting mixture stirred at rt for 30 minutes. The mixture was diluted with water (5.0 mL), and extracted with EtOAc (10 mL×3). The organic layers were combined, washed with brine (10 mL×2), dried (Na₂SO₄) and concentrated to provide a crude product, which was purified by flash chromatography to give the desired product (49 mg, 87%). ESI-MS m/z=555.23 [M+H]⁺.

Step 8d. To a mixture of the compound from Step 8c (20 mg, 0.036 mmol) in xylene (0.5 mL) in a heating tube was added NH₄OAc (42 mg, 0.54 mmol). The tube was then sealed and heated at 130° C. for 1 hour. The mixture was diluted with water (5.0 mL), and extracted with EtOAc. The organic layers were combined, dried (Na₂SO₄) and concentrated to provide a crude product, which was purified by flash chromatography to give the desired product (10 mg, 54%). ESI-MS m/z=535.26 [M+H]⁺.

Step 8e To a stirred solution of the compound from Step 8d (10 mg, 0.019 mmol) in THF (1.0 mL) was added a solution of TBAF in THF (0.16 mL, 1.0 M solution) at 0° C. The resulting mixture was then warmed up to rt and stirred at rt for 2 h. The mixture was diluted with aq. NaHCO₃ solution (5.0 mL), and extracted with EtOAc. The organic layers were combined, dried (Na₂SO₄) and concentrated to provide a crude product, which was purified by flash chromatography to give the title product (5.4 mg, 67%). ESI-MS m/z=421.16 [M+H]⁺.

Example 9

Step 9a. A solution of ethyl 3-aminoisoxazole-5-carboxylate (300 mg, 1.78 mmol) and Et₃N (719 mg, 7.12 mmol) in DCM (10 mL) was added dropwise to a solution of triphosgene (264.33 mg, 0.89 mmol) in DCM (10 mL) at −70° C. under N₂. The mixture was stirred at −70° C. for 0.5 hour. Then the mixture was added dropwise to a solution of 4-hydroxypiperidine (1.78 g, 17.8 mmol) in DCM (10 mL) at rt under N₂. The mixture was stirred at rt for 1 hour. Then it was concentrated and the residue was chromatographed (silica, DCM/MeOH) to give the desired compound as yellow oil (190 mg, 36%).

Step 9b. A mixture of the compound from step 9a (170 mg, 0.57 mmol) and LiOH (72.4 mg, 1.72 mmol) in methanol/H₂O (10 mL/2 mL) was stirred for 3 hours at rt. Then the solution was adjusted with HCl (2N) to PH=4, diluted with DCM and washed with aq NH₄Cl and brine. The organic layer was dried (Na₂SO₄), filtered and concentrated to give the desired compound as yellow oil (100 mg, 65%).

Step 9c. A mixture of the compound from Step 9b (100 mg, 0.39 mmol), 3,4,5-trifluoroaniline (63.4 mg, 0.43 mmol), HATU (222 mg, 0.58 mmol), DIEPA (151 mg, 1.17 mmol) in THF (5 mL) was stirred for 2 hours at rt. It was concentrated and the residue was partitioned (DCM-brine). The organic was dried (Na₂SO₄) filtered and concentrated. The residue was chromatographed (silica ethyl acetate/petroleum ether) to give the title compound as a white solid (45 mg, 30%) ESI-MS m/z=385 [M+H]⁺.

Example 10

Step 10a. A solution of ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate (100 mg, 0.59 mmol), triphosgen (122.87 mg, 0.41 mmol), TEA (238.76 mg, 2.36 mmol) in DCM (12 mL) was stirred for 30 minutes at −78° C. Then 4-hydroxypiperidine (89.54 mg, 0.88 mmol) was added into the above solution. The resulting solution was stirred for 30 minutes at room temperature. It was concentrated and the residue was chromatographed (silica, ethyl acetate/petroleum ether) to give the desired compound as light yellow solid (153.8 mg, 90%). ESI-MS m/z=297.20 [M+H]⁺.

Step 10b. A solution of the compound from step 10a (153.8 mg, 0.52 mmol), LiOH (49.92 mg, 2.08 mmol) in THF/H₂O (12 mL/3 mL) was stirred for 40 minutes at room temperature. It was concentrated and adjusted pH=5 by 1N HCl. It was filtered and dried in vacuum to give the desired compound as white solid (149.8 mg, 100%). ESI-MS m/z=269.30 [M+H]⁺.

Step 10c. A solution of compound from step 10b (149.8 mg, 0.55 mmol), 3,4,5-trifluorobenzamine (82.83 mg, 0.56 mmol), HATU (234.22 mg, 0.62 mmol), DIPEA (288.96 mg, 2.24 mmol) in DMF (5 mL) was stirred for 2 hours at room temperature. The organic layer was purified by Flash-Prep-HPLC (C₁₈ column, MeCN/H₂O) to give the title compound as white solid (54.2 mg, 24.76%). ESI-MS m/z=398.20 [M+H]⁺.

Example 11

Step 11a. A solution of the compound from step 8a (501.5 mg, 1.22 mmol), NCS (210.08 mg, 1.28 mmol), AIBN (11.35 mg, 0.08 mmol) in MeCN (5 mL) was stirred for 1.5 hours under N₂ atmosphere at room temperature. It was concentrated to give the desired compound as yellow oil (300 mg, 55%), which used directly to next step directly without further purification. ESI-MS m/z=445.35, 447.35 [M+H]⁺.

Step 11b. A solution of the compound from step 11a (300 mg, 0.67 mmol), LiOH (64.72 mg, 2.69 mmol) in THF/H₂O (10 mL/3.5 mL) was stirred for 40 minutes under N₂ atmosphere at room temperature. It was concentrated and adjusted pH=5 by 1 N HCl. It was filtered and dried in vacuum to give the desired compound as white solid (120 mg, 42.95%). ESI-MS m/z=417.10, 419.10 [M+H]⁺.

Step 11c. A solution of compound from step 11b (120 mg, 0.28 mmol), 3,4,5-trifluorobenzamine (41.16 mg, 0.28 mmol), HATU (127.75 mg, 0.33 mmol), NaHCO₃ (70.56 mg, 0.84 mmol) in DMF (5 mL) was stirred for 16 hours at room temperature. It was diluted with ethyl acetate and washed with brine. The organic was dried (Na₂SO₄), filtered and concentrated. The residue was purified by Flash chromatography (C₁₈ column, MeCN/H₂O) to give the desired compound as white solid (90 mg, 59%). ESI-MS m/z=546.20, 548.20 [M+H]⁺.

Step 11d. A solution of compound from step 11c (90 mg, 0.16 mmol) in DCM (5 mL) and TFA (0.5 mL) was stirred for 3 hours at room temperature. It was diluted with DCM and washed with brine. The organic phase was dried (Na₂SO₄), filtered and concentrated. The residue was purified by Prep-HPLC (MeCN/H₂O) to give the title compound as white solid (11.4 mg, 17%). ESI-MS m/z=432.15, 434.15 [M+H]⁺.

The following examples were prepared using procedures similar to that described above.

Mass Spectra. Examples Structure ESI-MS, (M + H)⁺ 12

524.25 13

398.20 14

397.15 15

359.00 16

382.2 17

400.00 18

418.00 19

412.0 20

384.0 21

372.0 22

368.0 23

418.0 24

372.3 25

385.0 26

382.0 27

402.0 28

410.15 29

384.0 30

370.0 31

370.0 32

358.3 33

424.1 34

362.0 35

378.10 36

414.05, 416.05 37

345.10 38

369.9 39

386.0 40

356.2 41

384.0 42

419.9 43

362.0 44

380.0 45

380.0 46

380.0 47

379.9 48

396.0, 398.0 49

396.0, 398.0 50

378.0 51

344.0 52

430.0 53

387.2 54

376.0 55

392.0 56

345.2 57

370.0 58

412.3 59

396.10, 398.10 60

413.95, 415.95 61

345.20 62

360.15 63

360.0 64

374.0 65

374.3 66

372.0 67

386.0 68

386.4 69

400.1 70

420.1 71

462.05, 464.05 72

402.0 73

402.3 74

388.4 75

372.0 76

400.0 77

420.4 78

434.1 79

434.0 Biological Activity

Methods: HepAD38 cells are maintained as previously reported (Ladner et al, Antimicrob. Agents Chemother. 1997, 4, 1715). Briefly, cells are passaged upon attaining confluency in DMEM/F12 media in the presence of 10% FBS, Penn/Strep, 250 μg/mL G418, and 1 μg/ml tetracycline. Novel compounds are screened by first washing cells three times with PBS to remove tetracycline, and plating in 96 well plates at 35,000 cells/well. Compounds dissolved in DMSO are then diluted 1:200 into wells containing cells. Five days after compound addition, material is harvested for analysis. For an extended 8 day analysis, cells are plated and treated as described above, but media and compound are refreshed on d2 and d5 post initial treatment.

On harvest day, virion DNA is obtained by lysing with Sidestep Lysis and Stabilization Buffer and then quantified via quantitative real time PCR. Commercially available ELISA kits are used to quantitate the viral proteins HBsAg (Alpco) or HbeAg (US Biological) by following the manufacturer's recommended protocol after diluting samples to match the linear range of their respective assays. Irrespective of readout, compound concentrations that reduce viral product accumulation in the cell lysates or supernatants by 50% relative to no drug controls (EC₅₀) are reported; EC₅₀ ranges are as follows: A<1 μM; B 1-10 μM; C>10 μM.

Compound toxicity is evaluated by seeding cells at 15,000 cells/well and treating with compound as described above. Three days after compound addition, cells are treated with ATPLite reagent and compound concentrations that reduce total ATP levels in wells by 50% relative to no drug controls (CC₅₀) are reported; CC₅₀ ranges are as follows: A>30 μM; B 10-30 μM; C<10 μM; D>10 μM.

TABLE 1 Summary of Activities HepAD38 CC₅₀ HepAD38 CC₅₀ Example EC₅₀ ATPlite Example EC₅₀ ATPlite 1 C A 2 B A 3 A A 4 B C 5 A A 6 C D 7 B A 8 C D 9 C C 10 C A 11 B A 12 B B 13 C D 14 B A 15 A A 16 B C 17 B C 18 B A 19 B A 20 B A 21 B A 22 C A 23 B C 24 B A 25 C A 26 A A 27 C A 28 A A 29 B C 30 A A 31 B A 32 B B 33 B A 34 B A 35 C A 36 C A 37 C A 38 A B 39 B A 40 B C 41 A A 42 B A 43 B A 44 B A 45 B A 46 C B 47 C A 48 B C 49 B A 50 C A 51 C A 52 B A 53 B A 54 A C 55 C A 56 C A 57 B C 58 C A 59 C A 60 B C 61 C A 62 C A 63 C A 64 C A 65 C A 66 C A 67 C A 68 C D 69 C A 70 C A 71 B A 72 C A 73 C A 74 C A 75 C A 76 C A 77 C C 78 C A 79 C A

While this invention has been particularly shown and described with references to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the scope of the invention encompassed by the appended claims. 

What is claimed is:
 1. A compound represented by Formula (I): X-A-Y—Z-L-R₁  (I), or a pharmaceutically acceptable salt thereof, wherein: X is an optionally substituted phenyl; A is —NHCO—; Y is selected from the groups set forth below,

wherein each group is optionally substituted and the amino group is connected to Z; or Y is selected from the groups below,

wherein each group is optionally substituted; the second connection point of Y is any carbon atom; and the amino group is connected to Z; Z is —C(O)—; L is —NR₂—; and R₁ and R₂ at each occurrence are independently selected from the group consisting of hydrogen, optionally substituted —C₁-C₈ alkyl, optionally substituted —C₂-C₈ alkenyl, optionally substituted —C₂-C₈ alkynyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted 3- to 8-membered heterocyclic, optionally substituted aryl and optionally substituted heteroaryl; alternatively, R₁ and R₂ are taken together with the atom to which they are attached to form an optionally substituted 3- to 8-membered heterocyclic.
 2. The compound of claim 1, wherein Y is selected from the following:

wherein each of the above shown groups is optionally substituted.
 3. The compound of claim 1, wherein Y is selected from the following:

wherein each of the above shown groups is optionally substituted and the second connection point of Y is at any carbon atom.
 4. The compound of claim 1, represented by Formula (IIb-5-B), or a pharmaceutically acceptable salt thereof:

wherein each R₁₅ is independently selected from the group consisting of hydroxy, halogen, cyano, —CO₂CH₃, —CO₂H, optionally substituted aryl, optionally substituted —C₁-C₆ alkyl, optionally substituted —C₃-C₈ cycloalkyl, optionally substituted —C₁-C₃ alkoxy; R₁₆ is independently selected from optionally substituted —C₁-C₆ alkyl and optionally substituted —C₃-C₈ cycloalkyl; and m is 1, 2, 3, 4 or
 5. 5. The compound of claim 1 selected from the compounds set forth below or a pharmaceutically acceptable salt thereof: Compound Structure  3

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6. A pharmaceutical composition, comprising a compound according to claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or excipient.
 7. The compound of claim 1, wherein X and Y are each optionally substituted with one to three substituents independently selected from the group consisting of halo, CN, and optionally substituted methyl.
 8. The compound of claim 7, wherein X is substituted with 1 to 3 fluorine atoms.
 9. The compound of claim 8, wherein X is 3,4,5-trifluorophenyl. 